Author: Sudheer vanguri

Base Medico Pvt. Ltd. is inviting applications for Officer / Senior Officer positions in its Formulation & Development department.
The vacancies are available at Tundav, Savli–Vadodara Road, Vadodara, Gujarat.
Candidates with relevant pharmaceutical qualifications and experience in formulation development, product development, and technology transfer can apply.
The company is offering a CTC of ₹3.00 LPA to ₹3.50 LPA for the advertised positions.

Company Overview

Base Medico Pvt. Ltd. is recruiting professionals for its Formulation & Development department. The role involves formulation development, pre-formulation studies, laboratory-scale development, scale-up activities, technology transfer, and coordination with the analytical department.

Base Medico Formulation & Development Jobs in Vadodara

Position Details

• Department: Formulation & Development
• Designation: Officer / Senior Officer
• Job Location: Tundav, Savli–Vadodara Road, Vadodara, Gujarat
• Salary: ₹3.00 LPA to ₹3.50 LPA

Job Role & Responsibilities

Formulation & Development Department

The selected candidates will be responsible for the following activities:

1. Supervise the Formulation & Development area and monitor the work of assistants and operators within the designated premises.
2. Conduct literature and patent searches and review the findings according to product requirements.
3. Characterize innovator and market samples.
4. Plan day-to-day execution of Formulation & Development trials for domestic, ROW, and other regulatory markets.
5. Handle characterization, laboratory-scale development, scale-up, technology transfer, and exhibit batches.
6. Plan pre-formulation studies for product development.
7. Execute development trials, achieve the desired critical quality attributes, and manufacture stability batches.
8. Improve existing formulations and explore the possibility of developing new dosage forms.
9. Ensure the timely completion of assigned formulation development and technology transfer activities.
10. Coordinate with the Analytical Department for routine analysis of formulations and development samples.

Eligibility & Qualifications

Candidates with relevant pharmaceutical qualifications and experience in formulation development are encouraged to apply.

Educational Qualifications

Candidates should have a relevant pharmaceutical qualification suitable for the Officer / Senior Officer position.

Relevant Experience and Skills

• Formulation and product development.
• Literature and patent searches.
• Innovator and market sample characterization.
• Pre-formulation studies.
• Laboratory-scale development and scale-up.
• Technology transfer and exhibit batch execution.
• Stability batch manufacturing.
• Understanding of critical quality attributes.
• Coordination with analytical laboratories.

Location & Salary

Job Location

Base Medico Pvt. Ltd.

Tundav, Savli–Vadodara Road, Vadodara, Gujarat.

Salary Details

The advertised CTC is ₹3.00 LPA to ₹3.50 LPA, depending on the applicable position and recruitment terms.

How to Apply

Interested candidates can send their updated CV to the recruitment email address below.

Email: hr@basemedico.com

Application Instructions

• Prepare an updated CV with relevant pharmaceutical experience.
• Highlight experience in Formulation & Development, product development, and technology transfer.
• Mention the designation of Officer / Senior Officer in the application.
• Send the CV to hr@basemedico.com.

Frequently Asked Questions

1. Which company is hiring for Formulation & Development positions?

Base Medico Pvt. Ltd. is recruiting candidates for its Formulation & Development department.

2. What is the designation offered?

The advertised designations are Officer and Senior Officer.

3. What salary is offered?

The advertised CTC ranges from ₹3.00 LPA to ₹3.50 LPA.

4. Where is the job located?

The position is based at Tundav, Savli–Vadodara Road, Vadodara, Gujarat.

5. What are the main responsibilities?

The role includes formulation development, pre-formulation studies, scale-up, technology transfer, stability batch manufacturing, and coordination with the analytical department.

6. How can candidates apply?

Candidates can email their updated CV to hr@basemedico.com.

Job Summary

Category	Details
Company	Base Medico Pvt. Ltd.
Vacancies	Officer / Senior Officer – Formulation & Development
Required Education	Relevant pharmaceutical qualification
Experience	Not specified in the recruitment information
Location	Tundav, Savli–Vadodara Road, Vadodara, Gujarat

Thermo Fisher Scientific Recruitment – FSP Associate Safety Specialist

Thermo Fisher Scientific is hiring an FSP – Associate Safety Specialist for a fully remote position in India. This opportunity is suitable for candidates interested in pharmacovigilance (PV), drug safety, adverse event reporting, and regulatory safety documentation. The role involves reviewing safety cases, entering and coding adverse event data, conducting follow-ups, and preparing regulatory safety reports within a highly regulated environment. Candidates with a relevant degree and experience comparable to 0–2 years can review the eligibility requirements and apply through the official careers portal.

Company Overview

Thermo Fisher Scientific provides scientific services and solutions to pharmaceutical and biotechnology companies. Its clinical research teams support drug development and patient safety through clinical research and pharmacovigilance activities.

This position focuses on day-to-day drug safety operations and accurate handling of safety information in accordance with applicable procedures and regulatory requirements.

Job Details

Job Role & Responsibilities

The selected candidate will perform day-to-day pharmacovigilance activities, including the collection, monitoring, assessment, evaluation, research, and tracking of safety information.

Key responsibilities include:

• Perform routine pharmacovigilance activities within a regulated environment and meet strict timelines.

• Enter and code adverse event data and support adverse event assessment.

• Review safety cases and conduct follow-up activities where required.

• Track safety reports and support regulatory reporting activities.

• Review cases for quality, consistency, and accuracy, including reports prepared by peers.

• Prepare and maintain regulatory safety reports.

• Review regulatory and pharmacovigilance publications to stay informed about current regulations, practices, procedures, and proposals.

• Maintain medical understanding of relevant therapeutic areas and disease states.

• Collaborate with project teams, client contacts, investigators, adverse event reporters, and third-party vendors.

• Participate in on-call duties for specific projects when required to support 24-hour case intake coverage from investigative sites.

Eligibility & Qualifications

Candidates should have a bachelor’s degree or equivalent qualification, along with relevant formal academic or vocational qualifications.

Relevant courses may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Nursing, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Microbiology, M.Sc. Microbiology, or other related healthcare and life sciences qualifications.

Experience Requirements

• Experience comparable to 0–2 years.

• Interest or relevant exposure to pharmacovigilance, drug safety, adverse event processing, or regulatory safety reporting may be useful for this role.

Required Skills

• Strong critical-thinking and problem-solving skills.

• Good written and verbal communication, including paraphrasing skills.

• Good command of English and the ability to translate information into a local language where required.

• Computer literacy and the ability to work across multiple databases.

• Familiarity with Microsoft Outlook, Word, and Excel.

• Understanding of medical terminology.

• Awareness of the importance of procedural documents and regulatory compliance.

• Ability to prioritize tasks and meet strict deadlines with limited supervision.

• Strong attention to detail.

• Ability to maintain a positive and professional approach in challenging situations.

• Ability to work effectively with a team to achieve shared goals.

Career Opportunity in Pharmacovigilance

This role offers exposure to core drug safety processes, including adverse event data entry, case review, safety report preparation, and regulatory reporting. It may be relevant to candidates looking to build experience in pharmacovigilance operations and clinical drug safety.

How to Apply

Interested candidates can apply through the official Thermo Fisher Scientific careers portal.

Apply here: FSP – Associate Safety Specialist | Thermo Fisher Scientific

Review the official job description for the latest application status and requirements before submitting your application.

Job Summary

Thermo Fisher Scientific Recruitment – Clinical Data Associate I

Thermo Fisher Scientific is hiring a Clinical Data Associate I (CDA I) for its clinical research operations in Bengaluru, India. This fully remote, full-time opportunity focuses on clinical data cleaning, discrepancy resolution, and data query management in accordance with Good Clinical Practice (GCP) and standard operating procedures. Candidates interested in clinical data management and clinical research data quality should review the educational and experience requirements carefully. The position requires experience comparable to at least four years, along with the relevant academic or vocational qualifications specified in the official posting.

Company Overview

Thermo Fisher Scientific supports pharmaceutical and biotechnology companies through scientific services and clinical research solutions. Its clinical research teams contribute to clinical trials by supporting data quality and processes used to assess the safety and efficacy of investigational products and medical devices.

Job Details

Job Role & Responsibilities

The selected candidate will perform entry-level clinical data cleaning activities while maintaining accuracy and following GCP requirements, global SOPs, work practice documents, and client expectations.

Key responsibilities include:

• Identify, resolve, and update clinical data discrepancies.

• Make changes to the data management database when required.

• Generate, track, and resolve data clarification requests and queries.

• Support the implementation of Case Report Form (CRF) designs in designated graphic design packages, where required.

• Maintain accuracy and consistency in clinical trial data.

• Follow project protocols and the Data Validation Manual.

• Handle clinical data and client proprietary information confidentially.

Eligibility & Qualifications

The official posting specifies the following educational requirements:

• High school or secondary school diploma, or equivalent, along with a relevant formal academic or vocational qualification.

• Technical positions may require a certificate.

• A combination of appropriate education, training, and directly related experience may be considered equivalent in some cases.

Experience Requirements

Candidates should have previous experience providing the knowledge, skills, and abilities required for the position, comparable to at least four years.

The supplied job description does not explicitly state that this experience must be in a specific clinical research or pharmaceutical role.

Required Skills

• Strong attention to detail and numerical accuracy.

• Ability to use interactive computer programs.

• Good written and verbal communication skills.

• Strong command of English language and grammar.

• Analytical thinking and problem-solving abilities.

• Ability to work productively under direct supervision.

• Ability to maintain confidentiality of clinical and client proprietary data.

• Flexibility and adaptability in changing work situations.

• Ability to work independently and collaboratively within a team.

• Sound judgment and decision-making skills.

• Understanding of project protocols and the Data Validation Manual.

• Ability to follow regulatory guidelines, global SOPs, and client expectations.

How to Apply

Interested candidates can apply through Thermo Fisher Scientific’s official careers portal.

Apply here: Clinical Data Associate I – Thermo Fisher Scientific

Review the official job description for the latest requirements and application status before submitting your application.

Job Summary

Fortrea Recruitment – Apprentice, Costing

Fortrea is inviting applications for the Apprentice – Costing position within its Clinical Costing Team in India. This opportunity is suitable for fresh graduates and candidates with qualifications in Life Sciences, Pharmacy, Nursing, Medicine, Biomedical Sciences, or Clinical Research. The role offers exposure to clinical research budgeting, drug development processes, clinical study planning, and analytical projects. Candidates interested in building a career in clinical research operations and costing can apply before 20 October 2026.

Company Overview

Fortrea is a global contract research organization (CRO) supporting pharmaceutical and biotechnology companies with clinical development services. Its Clinical Costing Team is part of the Enterprise Client Solutions function and develops clinical, monitoring, and resourcing strategies for late-stage client requests for proposals.

The team works to ensure that clinical study budget proposals are competitive, operationally sound, and feasible.

Job Details

Job Role & Responsibilities

The Apprentice will participate in entry-level departmental activities and follow Fortrea and/or sponsor Standard Operating Procedures (SOPs).

Key responsibilities include:

• Attend training sessions to learn about the drug development process and how clinical research is planned, conducted, and reported.

• Learn the tools and processes used by the Clinical Costing Team to prepare clinical study budgets.

• Support special projects and analytical activities.

• Participate in projects that may provide opportunities to present findings to senior management and support informed decision-making.

• Shadow senior team members to understand their daily activities and the strategies behind clinical research operations.

• Develop knowledge and skills related to clinical research costing and operational processes.

Eligibility & Qualifications

Candidates should have a bachelor’s or master’s degree in a relevant discipline.

Relevant qualifications include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Nursing, MBBS, Biomedical Sciences, Clinical Research, or equivalent qualifications aligned with the employer’s stated educational requirements.

Candidates with an Information Technology or informatics background and an interest in clinical research are also welcome to apply.

Preferred Qualifications & Skills

• Clinical research or ICH-GCP certification is preferred.

• Experience delivering projects in an academic setting.

• Good analytical and computing skills.

• Ability to collaborate and communicate effectively with internal and external stakeholders.

• Willingness to explore innovative approaches through collaboration and partnerships.

• Flexibility to work according to business requirements.

Career Opportunity in Clinical Research Costing

This apprenticeship provides an opportunity to learn how clinical study budgets are developed and how costing supports clinical research proposals. Candidates can gain exposure to drug development, clinical research planning, analytical projects, and cross-functional collaboration.

It may be particularly relevant for graduates looking to explore clinical research operations, clinical trial budgeting, and related CRO career pathways.

Work Location & Timings

The position is listed as remote, with Bangalore and Remote India shown as locations. Candidates should review the official job listing for the applicable work arrangement and any location-specific conditions.

The employer also expects apprentices to be open to flexible work timings.

How to Apply

Interested and eligible candidates can submit their applications through Fortrea’s official recruitment portal.

Application deadline: 20 October 2026

• Apply for Apprentice – Costing at Fortrea

• View the official job description

Review the official listing for the latest application status and requirements before applying.

Job Summary

Nayas Labs Pvt. Ltd. is hiring Officers and Executives for its Analytical Research & Development (AR&D) and Formulation Research & Development (FR&D) departments in Kukatpally, Hyderabad.
Candidates with M.Sc., M.Pharm, or B.Pharm qualifications can apply for the available positions.
AR&D applicants should have 1–4+ years of experience, while FR&D candidates should have 2–4+ years of experience.
Immediate joiners will be preferred for both departments.

Company Overview

Nayas Labs Pvt. Ltd. is recruiting professionals for analytical development and formulation development functions. The openings are intended for candidates with relevant pharmaceutical and analytical experience who can contribute to laboratory testing, analytical method development, and oral solid dosage formulation development.

Nayas Labs Analytical Research & Development (AR&D) Jobs in Hyderabad

Designation

Officer / Executive – Analytical Development

Eligibility & Qualifications

• Qualification: M.Sc. / M.Pharm / B.Pharm
• Experience: 1–4+ years
• Preferred Candidates: Immediate joiners will be preferred.

Job Profile & Responsibilities

• Develop analytical methods and analyse samples.
• Handle HPLC, dissolution, and other analytical tests.
• Calibrate and maintain laboratory instruments.

Nayas Labs Formulation Research & Development (FR&D) Jobs in Hyderabad

Designation

Officer / Executive – Formulation Development

Eligibility & Qualifications

• Qualification: M.Sc. / M.Pharm / B.Pharm
• Experience: 2–4+ years
• Preferred Candidates: Immediate joiners will be preferred.

Job Profile & Responsibilities

• Design and optimise drug formulations.
• Conduct pre-formulation studies and assess drug-excipient compatibility.
• Handle end-to-end formulation development for oral solid dosage forms.

Job Location

Nayas Labs Pvt. Ltd.

Kukatpally, Hyderabad, Telangana.

How to Apply

Interested candidates can share their updated CVs through the recruitment email addresses provided below.

• Email: sharad.chandra@jeevanscientific.com
• Email: HR@jeevanscientific.com

Candidates should mention their preferred department, relevant experience, and current availability when submitting their resumes.

Important Instructions

• Apply for the department matching your qualifications and experience.
• AR&D candidates should have experience in analytical method development, HPLC, dissolution testing, and laboratory instrument maintenance.
• FR&D candidates should have experience in formulation development, pre-formulation studies, and drug-excipient compatibility.
• Immediate joiners will be preferred for both positions.

Frequently Asked Questions

1. Which company is hiring for AR&D and FR&D positions?

Nayas Labs Pvt. Ltd. is recruiting Officers and Executives for Analytical Development and Formulation Development.

2. Which qualifications are accepted?

Candidates with M.Sc., M.Pharm, or B.Pharm qualifications can apply for the advertised positions.

3. How much experience is required for AR&D jobs?

Candidates should have 1–4+ years of experience in Analytical Development.

4. How much experience is required for FR&D jobs?

Candidates should have 2–4+ years of experience in Formulation Development.

5. Are immediate joiners preferred?

Yes. Immediate joiners will be preferred for both AR&D and FR&D positions.

6. How can candidates apply?

Candidates can email their updated CV to sharad.chandra@jeevanscientific.com or HR@jeevanscientific.com.

Job Summary

Category	Details
Company	Nayas Labs Pvt. Ltd.
Vacancies	Officer / Executive – Analytical Development; Officer / Executive – Formulation Development
Required Education	M.Sc., M.Pharm, B.Pharm
Experience	AR&D: 1–4+ years; FR&D: 2–4+ years
Location	Kukatpally, Hyderabad, Telangana

Akums is inviting experienced candidates to attend walk-in interviews for multiple positions at Pure & Cure Healthcare Pvt. Ltd. in Manakpur, Baddi, Himachal Pradesh.
The recruitment drive covers Production (OSD), Production (Liquid), Engineering, Quality Control, and Quality Assurance departments.
Candidates with B.Pharm, M.Pharm, ITI, Diploma, B.Tech, B.Sc., and M.Sc. (Chemistry) qualifications can apply for positions matching their experience.
The interviews are scheduled for 16 and 17 October 2026, from 10:00 AM to 3:00 PM.

Company Overview

Akums is recruiting experienced professionals for pharmaceutical manufacturing and quality-related operations at Pure & Cure Healthcare Pvt. Ltd., located in Manakpur, Baddi, Himachal Pradesh.

The vacancies cover pharmaceutical production, liquid manufacturing, engineering utilities, quality control, and quality assurance. Available designations range from Operator to Senior Executive, depending on the department and candidate experience.

Akums Production (OSD) Jobs in Baddi

Production Department Vacancies

Department: Production (OSD)

Sections:

• Documentation
• Manufacturing & Packing
• Strip & BQS

Designation: Operator to Senior Executive

Qualifications: B.Pharm / M.Pharm / ITI

Experience: 2–10 years

Akums Production (Liquid) Jobs in Baddi

Liquid Manufacturing Department Vacancy

Department: Production (Liquid)

Section: Liquid Oral

Designation: Officer to Assistant Executive

Qualifications: B.Pharm / M.Pharm

Experience: 1–5 years

Akums Engineering Jobs in Baddi

Engineering Department Vacancies

Department: Engineering

Sections:

• HVAC
• Water System
• Utility

Designation: Operator to Executive

Qualifications: B.Tech / Diploma in Mechanical or Electrical Engineering / ITI

Experience: 2–7 years

Akums Quality Control Jobs in Baddi

Quality Control Department Vacancies

Department: Quality Control

Sections:

• RM / PM / FG
• Stability
• GLP

Designation: Officer to Executive

Qualifications: B.Sc. / M.Sc. in Chemistry

Experience: 2–7 years

Akums Quality Assurance Jobs in Baddi

Quality Assurance Department Vacancies

Department: Quality Assurance

Sections:

• QMS
• Qualification
• IPQA
• Documentation

Designation: Officer to Executive

Qualification: B.Pharm

Experience: 2–7 years

Job Role & Responsibilities

Production (OSD)

Candidates applying for Production (OSD) positions may be considered for documentation, manufacturing and packing, and strip and BQS operations, according to the assigned role.

Production (Liquid)

The Liquid Production department has openings in liquid oral manufacturing. Applicants should have the required pharmaceutical qualification and relevant experience.

Engineering

Engineering vacancies cover HVAC systems, water systems, and utilities. Candidates should possess relevant technical qualifications and experience in the applicable engineering functions.

Quality Control

Quality Control vacancies cover raw materials, packaging materials, finished goods, stability testing, and GLP-related activities.

Quality Assurance

Quality Assurance vacancies cover QMS, qualification, IPQA, and documentation. Candidates should have relevant experience in pharmaceutical quality systems and compliance activities.

Eligibility & Qualifications

Candidates should possess the educational qualification and relevant experience specified for their preferred department.

Educational Qualifications

• B.Pharm
• M.Pharm
• ITI
• Diploma
• B.Tech
• B.Sc.
• M.Sc. in Chemistry
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering

Experience Requirements

• Production (OSD): 2–10 years.
• Production (Liquid): 1–5 years.
• Engineering: 2–7 years.
• Quality Control: 2–7 years.
• Quality Assurance: 2–7 years.

Candidates should check the department-wise requirements before applying.

Location & Salary

Interview Location

Pure & Cure Healthcare Pvt. Ltd.

Village Manakpur, PO Lodhimajra, Tehsil Baddi, District Solan, Himachal Pradesh.

Walk-In Interview Date & Timing

• Dates: 16 and 17 October 2026.
• Time: 10:00 AM to 3:00 PM.

Salary Details

The recruitment poster does not specify salary figures. Compensation may vary according to the designation, qualifications, and relevant experience.

How to Apply

Interested candidates can send their updated CV to the recruitment email address or contact the recruitment team for further information.

Email: recruit.pch3@akums.in

Contact Number: 9762401295

Documents to Carry

Candidates should keep the following documents ready for the recruitment process:

• Updated resume or CV.
• Educational qualification certificates.
• Relevant experience documents.

Candidates should confirm any additional document requirements with the recruitment team before attending.

Important Instructions

• Apply for positions matching your qualifications and experience.
• Check the required experience for your preferred department.
• Confirm the interview venue and timing before travelling.
• Contact the recruitment team if you need additional information about the vacancies.

Frequently Asked Questions

1. Which company is conducting the recruitment?

Akums is recruiting for positions at Pure & Cure Healthcare Pvt. Ltd. in Manakpur, Baddi, Himachal Pradesh.

2. Which departments have vacancies?

The openings are in Production (OSD), Production (Liquid), Engineering, Quality Control, and Quality Assurance.

3. Which qualifications are accepted?

The listed qualifications include B.Pharm, M.Pharm, ITI, Diploma, B.Tech, B.Sc., and M.Sc. in Chemistry, depending on the position.

4. Are freshers eligible for these positions?

The recruitment poster specifies experience requirements ranging from 1 to 10 years. Fresher vacancies are not listed.

5. When are the walk-in interviews scheduled?

The interviews are scheduled for 16 and 17 October 2026, from 10:00 AM to 3:00 PM.

6. How can candidates apply?

Candidates can send their CV to recruit.pch3@akums.in or contact 9762401295 for further information.

Job Summary

Category	Details
Company	Akums / Pure & Cure Healthcare Pvt. Ltd.
Vacancies	Production Operator, Production Executive, Engineering Operator / Executive, Quality Control Officer / Executive, Quality Assurance Officer / Executive
Required Education	B.Pharm, M.Pharm, ITI, Diploma, B.Tech, B.Sc., M.Sc. (Chemistry)
Experience	1–10 years, depending on the department
Location	Manakpur, Baddi, Solan, Himachal Pradesh

Brillex Clinical Research Pvt. Ltd. is hiring for the position of Executive / Manager – International Business Development for its clinical research organization.
The opportunity is intended for candidates with qualifications in B.Pharm, M.Pharm, Life Sciences, or MBA.
Applicants should have international business development experience in the CRO or pharmaceutical industry.
Interested candidates can apply by sending their updated resume to the recruitment email address provided below.

Company Overview

Brillex Clinical Research Pvt. Ltd. is a clinical research organization recruiting professionals for its international business development function. The advertised position focuses on candidates with relevant industry experience in business development within the Contract Research Organization (CRO) or pharmaceutical sector.

Brillex Clinical Research International Business Development Vacancy

Position Details

• Designation: Executive / Manager – International Business Development
• Department: International Business Development
• Industry: Clinical Research / Pharmaceutical
• Company: Brillex Clinical Research Pvt. Ltd.
• Experience: International business development experience in the CRO or pharmaceutical industry
• Job Location: 602, Ariane Legacy, Adalaj – Gandhinagar, Gujarat, India – 382421

Job Role & Responsibilities

The position is focused on international business development for a clinical research organization.

Candidates should have relevant experience in international business development within the CRO or pharmaceutical industry. The recruitment notice does not list specific day-to-day responsibilities, so applicants should confirm the detailed role expectations with the recruitment team.

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply, provided they have relevant international business development experience.

Educational Qualifications

• B.Pharm
• M.Pharm
• Life Sciences
• MBA

Experience Requirements

• International business development experience in the CRO or pharmaceutical industry.
• Relevant experience aligned with the Executive / Manager designation.

Location & Salary

Job Location

Brillex Clinical Research Pvt. Ltd.

602, Ariane Legacy, Adalaj – Gandhinagar, Gujarat, India – 382421.

Salary Details

The recruitment poster does not specify salary details. Compensation may depend on the designation, qualifications, and relevant professional experience.

How to Apply

Interested candidates can apply by sending their updated resume to the recruitment email address listed in the announcement.

Email: rushabhshah@brillexcro.com

Company Website: www.brillexcro.com

Application Instructions

• Prepare an updated resume highlighting international business development experience.
• Include relevant experience in the CRO or pharmaceutical industry.
• Mention the position of Executive / Manager – International Business Development in the application.
• Send the application to the recruitment email address.

Important Instructions

• Candidates should possess relevant international business development experience.
• Applicants should ensure their qualifications match the stated requirements.
• Candidates can contact the recruitment team for further details about the role and selection process.

Frequently Asked Questions

1. Which company is hiring for this position?

Brillex Clinical Research Pvt. Ltd. is recruiting for its international business development function.

2. What is the designation offered?

The advertised designation is Executive / Manager – International Business Development.

3. Which qualifications are accepted?

Candidates with B.Pharm, M.Pharm, Life Sciences, or MBA qualifications can apply.

4. Is experience required?

Yes. The recruitment notice requires international business development experience in the CRO or pharmaceutical industry.

5. How can candidates apply?

Candidates can send their updated resume to rushabhshah@brillexcro.com.

6. Where is the job located?

The address provided in the recruitment poster is 602, Ariane Legacy, Adalaj – Gandhinagar, Gujarat, India – 382421.

Job Summary

Category	Details
Company	Brillex Clinical Research Pvt. Ltd.
Vacancies	Executive / Manager – International Business Development
Required Education	B.Pharm, M.Pharm, Life Sciences, MBA
Experience	International business development experience in the CRO or pharmaceutical industry
Location	Adalaj – Gandhinagar, Gujarat, India

Annora Pharma Pvt. Ltd. is conducting a walk-in interview for experienced candidates at its Formulation OSD Unit in Annaram, Jinnaram, Hyderabad.
The recruitment drive includes vacancies in Engineering, Production, Packing, Quality Assurance, Quality Control, and Packing Development departments.
Candidates with ITI, Diploma, B.Sc., B.Tech, B.Pharm, and M.Pharm qualifications can apply for suitable positions based on the specified experience requirements.
The walk-in interview is scheduled for 17 October 2026, with opportunities for candidates having 2–7 years of relevant experience.

Company Overview

Annora Pharma Pvt. Ltd. is inviting experienced professionals to join its Formulation OSD Unit. The recruitment notice lists opportunities across pharmaceutical manufacturing, engineering, packing, quality assurance, quality control, and packing development.

The available designations include Technician, Junior Executive, Operator, Executive, Officer, and Designer & Commercial roles. Candidates should review the department-wise requirements before attending the interview.

Annora Pharma Engineering Jobs in Hyderabad

Engineering Department Vacancies

• Qualification: Diploma / B.Tech in Mechanical, ECE, or EEE.
• Experience: 2–6 years.
• Designation: Technician / Junior Executive.
• Area of Work: Process Electrical, Utility, and HVAC.

Annora Pharma Production Jobs in Hyderabad

Production Department Vacancies

• Qualification: ITI / Diploma / B.Sc.
• Experience: 2–6 years.
• Designation: Operator / Junior Executive.
• Area of Work: Granulation, compression, FBP, coating, capsule filling, and inspection.

Annora Pharma Packing Jobs in Hyderabad

Packing Department Vacancies

• Qualification: ITI / Diploma / B.Sc.
• Experience: 2–6 years.
• Designation: Operator / Junior Executive.
• Area of Work: Bottle and blister packing, sachet filling, and liquid manufacturing filling.

Annora Pharma Quality Assurance Jobs in Hyderabad

Quality Assurance Department Vacancy

• Qualification: B.Pharm / M.Pharm.
• Experience: 5–7 years.
• Designation: Junior Executive / Executive.
• Area of Work: IPQA.

Annora Pharma Quality Control Jobs in Hyderabad

Quality Control Department Vacancy

• Qualification: B.Pharm / M.Pharm.
• Experience: 2–6 years.
• Designation: Officer / Executive.
• Area of Work: Stability, GLP, IP/FP, and LIMS.

Annora Pharma Packing Development Jobs in Hyderabad

Packing Development Department Vacancy

• Qualification: Diploma in Packing.
• Experience: 3–6 years.
• Designation: Executive.
• Area of Work: Designer & Commercial.

Job Role & Responsibilities

Engineering Department

Engineering candidates will work in areas related to process electrical systems, utilities, and HVAC. Applicants should have relevant technical qualifications and experience in the applicable engineering functions.

Production Department

Production candidates should have experience in pharmaceutical manufacturing operations, including granulation, compression, fluid bed processing (FBP), coating, capsule filling, and inspection.

Packing Department

Packing candidates should have relevant experience in bottle packing, blister packing, sachet filling, and liquid manufacturing filling operations.

Quality Assurance Department

Quality Assurance candidates should have experience in In-Process Quality Assurance (IPQA) and related pharmaceutical quality activities.

Quality Control Department

Quality Control candidates should have experience in stability testing, Good Laboratory Practice (GLP), in-process and finished-product testing (IP/FP), and Laboratory Information Management Systems (LIMS).

Packing Development Department

Packing Development candidates should have a Diploma in Packing and relevant experience in the listed Designer & Commercial function.

Eligibility & Qualifications

Candidates should possess the relevant educational qualification and professional experience required for their preferred department.

Educational Qualifications

• ITI
• Diploma
• Diploma in Packing
• B.Sc.
• B.Tech in Mechanical Engineering
• B.Tech in Electronics and Communication Engineering (ECE)
• B.Tech in Electrical and Electronics Engineering (EEE)
• B.Pharm
• M.Pharm

Experience Requirements

• Engineering: 2–6 years.
• Production: 2–6 years.
• Packing: 2–6 years.
• Quality Assurance: 5–7 years.
• Quality Control: 2–6 years.
• Packing Development: 3–6 years.

Candidates should check the department requirements carefully before applying.

Location & Salary

Job Location

Annora Pharma Pvt. Ltd.

Sy. No. 261, Plot Nos. 13 and 14, Annaram Village, Jinnaram, Hyderabad.

Interview Date & Timing

• Date: 17 October 2026, Saturday.
• Time: 9:00 AM to 2:00 PM.

Salary Details

The recruitment poster does not specify salary figures. Compensation may vary according to the position, qualifications, and relevant experience.

How to Apply

Interested candidates should attend the walk-in interview with their updated resume and supporting documents.

Candidates who require additional information can contact the recruitment representative or send their resume to the email address provided in the recruitment notice.

Email: Sruthi.k@hetero.com

Contact Number: 8977546374

Documents to Carry

Candidates should bring the following documents to the interview:

• Latest increment letter.
• Recent salary slips.
• Academic documents.
• Identity proof.

Important Instructions

• Review the department-wise eligibility criteria before attending.
• Carry all required documents.
• Use the location QR code in the original recruitment poster to confirm the venue.
• Contact the recruitment representative for further information.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Annora Pharma Pvt. Ltd. is conducting recruitment for its Formulation OSD Unit.

2. Which qualifications are accepted?

The listed qualifications include ITI, Diploma, Diploma in Packing, B.Sc., B.Tech, B.Pharm, and M.Pharm, depending on the position.

3. Are freshers eligible for these vacancies?

The recruitment poster lists experience requirements ranging from 2 to 7 years. Fresher vacancies are not specified.

4. When is the walk-in interview scheduled?

The interview is scheduled for 17 October 2026, from 9:00 AM to 2:00 PM.

5. What is the salary offered?

The recruitment poster does not specify salary details. Candidates should confirm compensation during the recruitment process.

6. How can candidates obtain further information?

Candidates can contact 8977546374 or email Sruthi.k@hetero.com for further information.

Job Summary

Category	Details
Company	Annora Pharma Pvt. Ltd.
Vacancies	Technician, Junior Executive, Operator, Executive, Officer, Designer & Commercial
Required Education	ITI, Diploma, B.Sc., B.Tech, B.Pharm, M.Pharm
Experience	2–7 years, depending on the position
Location	Annaram, Jinnaram, Hyderabad

Torrent Pharmaceuticals is conducting a walk-in interview for experienced candidates at its manufacturing facility in Dahej, Gujarat.
The recruitment drive includes vacancies in Tablet Manufacturing, Packaging, Quality Control, Quality Assurance, and Engineering departments.
Candidates with ITI, SSC, HSC, B.Pharm, B.Sc., M.Pharm, M.Sc., Diploma, and B.E. qualifications can apply for suitable positions based on the specified requirements.
The walk-in interview is scheduled for 17 October 2026, with opportunities for candidates having 2–8 years of relevant pharmaceutical industry experience.

Company Overview

Torrent Pharmaceuticals is a pharmaceutical company offering career opportunities across manufacturing, packaging, quality, and engineering functions. The current recruitment notice lists experienced positions at its manufacturing facility in Dahej, Gujarat.

The vacancies include Technician, Technical Assistant / Executive, and Executive positions. Candidates should review the department-wise job responsibilities and qualifications before attending the interview.

Torrent Pharma Tablet Manufacturing Jobs in Dahej, Gujarat

Tablet Department Vacancies

1. Technician

• Qualification: ITI / SSC / HSC
• Experience: 2–8 years
• Job Responsibilities: Experience in Fette and Sejong compression machines, Glatt and PAM Glatt coaters, Viswill camera inspection machines, and granulation equipment operation.

2. Technical Assistant / Executive

• Qualification: B.Pharm / M.Pharm / M.Sc.
• Experience: 2–8 years
• Job Responsibilities: Experience in inline documentation, BMR, QMS, and related manufacturing activities.

Torrent Pharma Packaging Jobs in Dahej, Gujarat

Packaging Department Vacancies

1. Technician

• Qualification: ITI / SSC / HSC
• Experience: 2–8 years
• Job Responsibilities: Experience in BQS / Romaco blister packing machines, automatic cartonators, machine changeovers, and carton packing machine operations.

2. Technical Assistant / Executive

• Qualification: B.Pharm / B.Sc. / M.Pharm / M.Sc.
• Experience: 2–8 years
• Job Responsibilities: Experience in QMS, track and trace systems such as Optel / ACG, and serialization systems.

Torrent Pharma Quality Control Jobs in Dahej, Gujarat

Quality Control Department Vacancy

Technical Assistant / Executive

• Qualification: M.Sc. / B.Sc.
• Experience: 2–8 years
• Job Responsibilities: Experience in method validation, method transfer, RM testing, GC, and LPG investigation-related activities.

Torrent Pharma Quality Assurance Jobs in Dahej, Gujarat

Quality Assurance Department Vacancy

Technical Assistant / Executive

• Qualification: M.Pharm / B.Pharm
• Experience: 2–8 years
• Job Responsibilities: Experience in documentation, training, and process validation.

Torrent Pharma Engineering Jobs in Dahej, Gujarat

Engineering Department Vacancies

1. Technician

• Qualification: ITI / Diploma
• Experience: 2–8 years
• Job Responsibilities: Relevant experience in pharmaceutical engineering and plant maintenance activities.

2. Executive

• Qualification: B.E. in Mechanical / Instrumentation / Electrical
• Experience: 2–8 years
• Job Responsibilities: Experience in DSD (Tablet & Capsules) plant maintenance.

Job Role & Responsibilities

Manufacturing and Packaging

Candidates applying for manufacturing and packaging positions should have hands-on experience with pharmaceutical equipment and production operations. Relevant experience may include compression, coating, granulation, blister packing, carton packing, machine changeovers, and serialization systems.

Quality Control

Quality Control candidates should have relevant experience in method validation, method transfer, raw material testing, and the laboratory activities specified for the position.

Quality Assurance

Quality Assurance applicants should have experience in documentation, training, process validation, and applicable quality management systems.

Engineering

Engineering candidates should have relevant experience in plant maintenance and the operation or maintenance of pharmaceutical manufacturing equipment. The Executive position requires a B.E. qualification in Mechanical, Instrumentation, or Electrical engineering.

Eligibility & Qualifications

Candidates should possess the relevant educational qualification and pharmaceutical industry experience required for their preferred position.

Educational Qualifications

• ITI
• SSC
• HSC
• B.Pharm
• B.Sc.
• M.Pharm
• M.Sc.
• Diploma
• B.E. in Mechanical Engineering
• B.E. in Instrumentation Engineering
• B.E. in Electrical Engineering

Experience Requirements

The recruitment poster lists 2–8 years of experience for the advertised positions. Candidates should have relevant experience in the department and equipment or processes associated with the role.

Additional Eligibility Criteria

• Experience in the pharmaceutical industry is required.
• Candidates should have relevant experience for the advertised position.
• Applicants should carry the requested documents to the interview.
• Candidates attending the walk-in interview should be prepared to provide their employment and qualification details.

Location & Salary

Job Location

Torrent Pharmaceuticals Limited

Plot No. 810, Sector III, Industrial Area, Pithampur, Dist. Dhar – 454775, Madhya Pradesh, India.

Interview Date: 17 October 2026, Saturday
Interview Time: 9:00 AM to 4:00 PM

Important location note: The poster heading mentions Dahej, Gujarat, but the venue printed in the interview section gives an address in Pithampur, Madhya Pradesh. Candidates should scan the location QR code or contact the recruitment team to confirm the correct venue before travelling.

Salary Details

The recruitment poster does not specify salary figures. Compensation may vary according to the position, qualifications, and relevant experience.

How to Apply

Interested candidates should attend the walk-in interview after confirming the correct venue and preparing the required documents.

Candidates who cannot attend the interview may send their updated CV to the recruitment email address provided in the poster.

Email: hrdahej@torrentpharma.com

Documents to Carry

Candidates attending the interview should bring:

• Updated resume.
• Last six months’ salary slips.
• Latest CTC breakup.
• Previous experience letters.
• Educational qualification certificates.
• Mark sheets.
• PAN card.
• Aadhaar card.
• Passport-size photographs.

Contact Details

• Manufacturing and Packaging: +91 6357406095
• Quality Control and Quality Assurance: +91 7069039414
• Engineering: +91 7069039411

Important Instructions

• Candidates should have experience in the pharmaceutical industry relevant to the position.
• Applicants are requested to carry the required documents.
• Candidates should verify the interview venue before travelling because the poster contains conflicting location information.
• Torrent Pharmaceuticals does not engage any third party or agency to recruit candidates for this purpose.
• No amount is charged or accepted as a security deposit during the selection process.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Torrent Pharmaceuticals is conducting recruitment for Tablet Manufacturing, Packaging, Quality Control, Quality Assurance, and Engineering positions.

2. Which qualifications are accepted?

The listed qualifications include ITI, SSC, HSC, B.Pharm, B.Sc., M.Pharm, M.Sc., Diploma, and B.E. in Mechanical, Instrumentation, or Electrical engineering, depending on the position.

3. Are freshers eligible for these vacancies?

The recruitment notice lists 2–8 years of experience. Freshers are not specifically included in the advertised requirements.

4. When is the walk-in interview scheduled?

The interview is scheduled for 17 October 2026, from 9:00 AM to 4:00 PM.

5. What is the salary offered?

The recruitment poster does not mention salary details. Candidates should confirm compensation during the recruitment process.

6. How can candidates apply if they cannot attend?

Candidates who cannot attend the walk-in interview may send their updated CV to hrdahej@torrentpharma.com.

Job Summary

Category	Details
Company	Torrent Pharmaceuticals
Vacancies	Technician, Technical Assistant / Executive, Executive
Required Education	ITI, SSC, HSC, B.Pharm, B.Sc., M.Pharm, M.Sc., Diploma, B.E.
Experience	2–8 years
Location	Recruitment heading: Dahej, Gujarat; printed venue: Pithampur, Madhya Pradesh

Centaur Pharmaceuticals is conducting a walk-in interview for experienced candidates across Production, Packing, Quality Assurance, Quality Control, Warehouse, Engineering, and HR departments.
The recruitment drive is scheduled for 18 October 2026 at the company’s OSD Formulations Plants in Tuem, Goa, and Hinjewadi, Pune.
Candidates with B.Pharm, B.Sc., B.E./M.E., BCA, BBA, B.Com, Diploma, and other relevant qualifications can apply for suitable positions based on the requirements.
Applicants should review the department-wise vacancies, experience criteria, interview timings, and mandatory QR code registration process before attending.

Company Overview

Centaur Pharmaceuticals is inviting experienced professionals to explore career opportunities across its pharmaceutical manufacturing and support functions. The recruitment notice lists vacancies at two locations: Tuem, Goa, and Hinjewadi, Pune.

The openings cover Production, Packing, Quality Assurance, Quality Control, Warehouse, Engineering, and HR. The listed designations include Officer, Operator, Senior Officer, Executive, Assistant Manager, and Manager.

Centaur Pharmaceuticals Production Jobs in Tuem, Goa

Production Department Vacancies

• Granulation: Officer | B.Pharm | 3–8 years of experience
• Granulation: Operator | Diploma | 3–8 years of experience
• Compression: Officer | B.Pharm | 3–8 years of experience
• Compression: Operator | Diploma | 3–8 years of experience
• Tablet Coating: Operator | Diploma | 3–8 years of experience
• Wruster Coating: Operator | Diploma | 3–8 years of experience
• Roll Compactor: Operator | Diploma | 3–8 years of experience

Centaur Pharmaceuticals Packing Jobs in Tuem, Goa

Packing Department Vacancies

• Blister Primary Packing: Officer | B.Pharm | 3–8 years of experience
• Blister Primary Packing: Operator | Diploma | 3–8 years of experience
• Cartonator: Operator | Diploma | 3–8 years of experience
• Secondary Packing: Operator | Diploma | 3–8 years of experience
• Primary Packing: Operator | Diploma | 3–8 years of experience

Centaur Pharmaceuticals Quality Assurance Jobs in Tuem, Goa

Quality Assurance Department Vacancies

• IPQA: Officer / Executive | B.Pharm | 3–8 years of experience
• Process Validation: Senior Officer / Executive | B.Pharm | 5–8 years of experience
• Cleaning Validation: Senior Officer / Executive | B.Pharm | 5–8 years of experience
• QMS: Senior Officer / Executive | B.Pharm | 5–8 years of experience
• AQA: Senior Officer / Executive | B.Pharm | 3–7 years of experience
• Technology Transfer: Senior Officer / Executive | B.Pharm | 3–7 years of experience

Centaur Pharmaceuticals Quality Control Jobs in Tuem, Goa

Quality Control Department Vacancies

• Stability: Officer / Senior Officer | M.Sc. | 3–8 years of experience
• AMV: Officer / Senior Officer | M.Sc. | 3–8 years of experience
• IP / FP: Officer / Senior Officer | M.Sc. | 3–8 years of experience
• Microbiology: Officer / Senior Officer | M.Sc. | 3–8 years of experience

Centaur Pharmaceuticals Warehouse Jobs in Tuem, Goa

Warehouse Department Vacancy

• RM / PM Dispensing: Officer / Senior Officer | B.Sc. / B.Pharm | 2–7 years of experience

Centaur Pharmaceuticals Engineering Jobs in Tuem, Goa

Engineering Department Vacancy

• Process: Officer / Senior Officer | B.E. / M.E. | 3–7 years of experience

Centaur Pharmaceuticals HR Jobs in Tuem, Goa

Human Resources Department Vacancy

• Administration: Officer / Executive | BCA / BBA / B.Com | 3–7 years of experience

Centaur Pharmaceuticals Quality Control Jobs in Hinjewadi, Pune

Quality Control Section Head Vacancies

• RM – Section Head: Assistant Manager / Manager | M.Sc. | 12–16 years of experience
• Stability – Section Head: Assistant Manager / Manager | M.Sc. | 12–16 years of experience
• AMV / AMT – Section Head: Assistant Manager / Manager | M.Sc. | 12–16 years of experience
• GLP – Section Head: Assistant Manager / Manager | M.Sc. | 12–16 years of experience

Centaur Pharmaceuticals Quality Assurance Jobs in Hinjewadi, Pune

Quality Assurance Department Vacancies

• TT (TTQA): Senior Officer / Executive | B.Pharm / M.Pharm | 3–7 years of experience
• AQA: Senior Officer / Executive | B.Pharm / M.Pharm | 3–7 years of experience
• QMS: Senior Officer / Executive | B.Pharm / M.Pharm | 3–7 years of experience

Job Role & Responsibilities

Production and Packing Roles

Candidates applying for Production and Packing positions should have relevant experience in pharmaceutical manufacturing operations. The listed sections include granulation, compression, tablet coating, roll compactor operations, blister packing, cartonating, primary packing, and secondary packing.

Quality Assurance Roles

Quality Assurance vacancies cover IPQA, process validation, cleaning validation, QMS, AQA, and technology transfer. Candidates should have relevant experience in the applicable quality systems and processes.

Quality Control Roles

Quality Control positions cover stability, analytical method validation (AMV), IP/FP, microbiology, raw material testing, and section-head responsibilities. Candidates applying for senior management positions should meet the stated experience requirements.

Warehouse, Engineering and HR Roles

The Warehouse opening covers raw material and packaging material dispensing. The Engineering vacancy is for process-related work, while the HR opening covers administration. Applicants should have relevant experience and the qualification specified for their respective roles.

Eligibility & Qualifications

Candidates should possess the relevant educational qualification and professional experience required for their preferred position.

Educational Qualifications

• B.Pharm
• M.Pharm
• B.Sc.
• Diploma
• B.E. / M.E.
• BCA
• BBA
• B.Com
• M.Sc.

Experience Requirements

• Production and Packing: 3–8 years.
• Quality Assurance, Tuem, Goa: 3–8 years, depending on the role.
• Quality Control, Tuem, Goa: 3–8 years.
• Warehouse: 2–7 years.
• Engineering: 3–7 years.
• HR / Administration: 3–7 years.
• Quality Assurance, Hinjewadi, Pune: 3–7 years.
• Quality Control Section Head positions, Hinjewadi, Pune: 12–16 years.

Additional Eligibility Criteria

According to the recruitment notice:

• Candidates should have experience in relevant pharmaceutical manufacturing operations.
• Exposure to an OSD or regulated pharmaceutical plant is required.
• Experience in a USFDA- or EU-GMP-regulated environment is preferred.
• Candidates should be flexible to work in shifts.
• Knowledge of cGMP and GDP practices is relevant to the listed roles.
• Experience in QMS, deviations, and investigations is useful for applicable positions.
• HPLC and GC knowledge is relevant for Quality Control roles.

Location, Interview Date & Timing

Tuem, Goa

Interview Date: 18 October 2026, Sunday
Interview Time: 9:00 AM to 4:00 PM
Venue: Centaur Pharmaceuticals, Pvt. Ltd., Plot No. 60, Phase II, Tuem Industrial Estate, Pernem, Goa 403 512.

Hinjewadi, Pune

The recruitment notice lists Quality Assurance and Quality Control vacancies at the Hinjewadi OSD Formulations Plant. Candidates should use the location QR code on the original poster to confirm the venue and travel details.

Salary Details

The recruitment poster does not specify salary figures. Compensation may vary according to the designation, qualifications, and relevant experience.

How to Apply

Interested candidates should complete the mandatory registration process before attending the walk-in interview.

Registration Process

1. Scan the registration QR code provided in the recruitment poster.
2. Complete the registration process and provide accurate details.
3. Scan the location QR code to check the interview venue.
4. Prepare an updated resume and the required supporting documents.
5. Attend the interview at the appropriate location and within the stated time.

Important: QR code registration is mandatory according to the recruitment notice.

Candidates Unable to Attend the Walk-In Interview

Candidates who cannot attend the interview can send their updated resumes to the respective recruitment email addresses:

• For Goa (Tuem): tuem_hr@centaurgoa.com
• For Pune (Hinjewadi): hrpune@centaur.co.in

Documents to Carry

Candidates should bring the following documents:

• Updated resume.
• Passport-size photograph.
• Last three months’ salary slips.
• Appointment letter or increment letters.
• Educational certificates, original and photocopy.
• Identity proof.

Important Instructions

• This is a walk-in interview. No TA/DA will be provided.
• Candidates are requested to reach the venue on time.
• QR code registration is mandatory.
• Candidates should verify the correct interview location before travelling.
• Applicants should carry the documents listed in the recruitment poster.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Centaur Pharmaceuticals is conducting recruitment for Production, Packing, Quality Assurance, Quality Control, Warehouse, Engineering, and HR positions.

2. Which qualifications are accepted?

The listed qualifications include B.Pharm, M.Pharm, B.Sc., M.Sc., Diploma, B.E./M.E., BCA, BBA, and B.Com, depending on the position.

3. Are freshers eligible for these vacancies?

The recruitment poster lists experience requirements ranging from 2 to 16 years, depending on the position. Fresher vacancies are not listed.

4. When is the walk-in interview scheduled?

The recruitment poster specifies 18 October 2026, Sunday, from 9:00 AM to 4:00 PM.

5. Is QR code registration compulsory?

Yes. The recruitment notice states that QR code registration is mandatory.

6. What should candidates carry to the interview?

Candidates should carry an updated resume, passport-size photograph, last three months’ salary slips, appointment or increment letters, educational certificates, and identity proof.

Job Summary

Category	Details
Company	Centaur Pharmaceuticals
Vacancies	Production Officer, Production Operator, Packing Officer, Packing Operator, Quality Assurance Officer / Executive, Quality Control Officer / Senior Officer, Warehouse Officer, Engineering Officer, HR Officer / Executive, Assistant Manager, Manager
Required Education	B.Pharm, M.Pharm, B.Sc., M.Sc., Diploma, B.E. / M.E., BCA, BBA, B.Com
Experience	2–16 years, depending on the position
Location	Tuem, Goa; Hinjewadi, Pune