Author: Sudheer vanguri

Johnson & Johnson Recruitment – Scientist Pharmacometrics Support

Johnson & Johnson (J&J) is hiring a Scientist Pharmacometrics Support professional for its Clinical Pharmacology & Pharmacometrics (CPP) team in Hyderabad, India. This opportunity is suitable for candidates with a scientific degree and 1–3 years of pharmaceutical industry experience. The role focuses on pharmacokinetic (PK) and pharmacodynamic (PD) data preparation, dataset quality control, modelling support, and regulatory e-submission activities. Candidates with basic R programming skills and an understanding of clinical pharmacology, SDTM, ADaM, and clinical drug development can explore this opportunity.

Company Overview

Johnson & Johnson is a global healthcare company operating across Innovative Medicine and MedTech. Its research and development teams work to discover and develop treatments, improve patient outcomes, and advance healthcare innovation.

The Clinical Pharmacology & Pharmacometrics team supports drug development through pharmacokinetic and pharmacodynamic modelling, simulation, data analysis, and regulatory submission activities.

Job Details

Job Role & Responsibilities

The selected candidate will provide technical and operational support to Clinical Pharmacology and Pharmacometrics leaders across therapeutic areas. The role involves preparing analysis-ready datasets, performing quality checks, and supporting global regulatory submissions under the oversight of a senior Pharmacometrics Support Programmer.

Key responsibilities include:

• Prepare analysis-ready datasets for pharmacokinetic (PK) and/or pharmacodynamic (PD) analyses following interim and final database releases.

• Support datasets used for ADNCA and NONMEM analyses.

• Perform basic pharmacometrics analysis quality control (QC) activities.

• Document QC checks, findings, and follow-up actions.

• Support global regulatory submissions by preparing population PK/PD and Exposure-Response e-submission packages.

• Prepare datasets, control files, outputs, tables, and supporting documentation for regulatory submissions.

• Assist with process improvement initiatives, software validation, and technology enhancements.

• Follow applicable standard operating procedures (SOPs), regulatory requirements, and Johnson & Johnson Credo principles.

• Collaborate with CPP scientists, clinical pharmacology leaders, data management, clinical and statistical programming, bioanalysis, regulatory, and publishing teams.

• Coordinate with external stakeholders and pharmacokinetics office vendors when required.

Eligibility & Qualifications

Candidates must have a bachelor’s degree or equivalent qualification in a scientific discipline.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Chemistry, M.Sc. Chemistry, or related scientific qualifications. These are examples of potentially relevant courses; the official posting does not provide an exhaustive list of accepted degrees.

Experience Requirements

• 1–3 years of pharmaceutical industry experience.

• Experience in clinical pharmacology, pharmacometrics, or data analysis support roles is preferred.

• Understanding of clinical drug development processes.

• Familiarity with clinical data structures and pharmacokinetic analysis requirements.

Technical Skills Required

• R programming: Basic proficiency in R for data manipulation.

• Clinical data standards: Basic understanding of SDTM and ADaM data structures.

• Pharmacokinetic analysis: Basic understanding of ADNCA and NONMEM input dataset requirements.

• Pharmacometric modelling: Understanding of non-linear mixed-effects modelling.

• Clinical pharmacology: Knowledge of clinical PK and PK/PD concepts.

• Regulatory submissions: Ability to support preparation of datasets and documentation for global e-submissions.

Non-Technical Skills

• Clear written and verbal communication skills.

• Strong attention to detail and a quality-focused mindset.

• Ability to work effectively with cross-functional teams.

• Good planning, prioritization, and multitasking skills.

• Accountability for timely completion of assigned tasks.

• Willingness to learn and contribute to process improvement.

• Cultural awareness and the ability to collaborate with global teams.

• Ability to work independently under appropriate oversight.

• Fluency in English; local language requirements may apply.

Work Location & Arrangement

The position is based in Hyderabad, India, and is listed as a hybrid-work opportunity. The role involves collaboration with local and global teams and may require approximately 5% travel.

Career Opportunity in Pharmacometrics

This position provides an opportunity to develop expertise in clinical pharmacology, pharmacokinetic and pharmacodynamic data analysis, and regulatory submission support. It may suit early-career professionals interested in pharmacometrics, clinical data programming, pharmacokinetic modelling, and pharmaceutical research and development.

How to Apply

Interested candidates can review the full job description and submit their applications through the official Johnson & Johnson careers portal.

Apply here: Scientist Pharmacometrics Support – Hyderabad | Johnson & Johnson

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

Job Summary

Parexel Recruitment – Senior Data Surveillance Analyst

Parexel is hiring a Senior Data Surveillance Analyst for its Clinical Trials team in India, with Hyderabad as the primary location and Bengaluru as an additional location. This opportunity is suitable for experienced professionals in clinical research, clinical data analytics, and risk-based quality management (RBQM). The role involves centralized monitoring of clinical trials, analysis of Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs), and the use of programming tools to improve data analysis and reporting. Candidates with at least 4 years of biotechnology or pharmaceutical industry experience and 2 years of RBQM experience can review the eligibility requirements.

Company Overview

Parexel is a global clinical development partner providing clinical research and consulting solutions to the life sciences industry. The company collaborates with biopharmaceutical companies and research sites to design and deliver clinical trials, with a focus on patient safety, research quality, and the development of new therapies.

Job Details

Job Role & Responsibilities

The Senior Data Surveillance Analyst will lead centralized monitoring activities for global and complex clinical trials. The role involves configuring and maintaining Risk-Based Quality Management (RBQM) systems, analyzing clinical trial data, and supporting regulatory compliance.

Key responsibilities include:

• Act as a subject matter expert in the configuration, implementation, and execution of centralized monitoring RBQM systems across studies.

• Maintain Key Risk Indicator (KRI) and Quality Tolerance Limit (QTL) libraries within the RBQM platform.

• Coordinate with functional and cross-functional stakeholders to develop centralized monitoring configuration specifications.

• Provide operational expertise, training, and guidance on RBQM systems and serve as an escalation point for centralized monitoring issues.

• Conduct centralized monitoring reviews and interpret KRI and KPI data to provide actionable insights.

• Use programming languages such as R, SQL, or SAS to develop custom analyses, automate workflows, and integrate data systems.

• Support improvements to technologies, systems, processes, and training materials used in centralized monitoring and RBQM.

• Participate in process improvement initiatives and contribute to innovation in centralized monitoring.

• Help improve study execution, data accuracy, patient safety, and clinical trial performance.

Eligibility & Qualifications

Candidates should have a bachelor’s degree or equivalent experience in a related field.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, Statistics, Biostatistics, Data Science, Clinical Research, or related scientific and analytical disciplines. These are examples of potentially relevant qualifications; the official posting does not provide an exhaustive list of accepted degrees.

Experience Requirements

Applicants must meet the following requirements:

• At least 4 years of relevant biotechnology or pharmaceutical industry experience.

• A minimum of 2 years of direct experience with RBQM systems or similar centralized monitoring platforms.

• Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.

• Advanced proficiency in Microsoft Excel for data manipulation and reporting.

Preferred Qualifications

• A master’s degree in a related field, such as Data Science, Biostatistics, or Clinical Research.

• Experience with CluePoints or similar centralized monitoring and RBQM solutions.

• Experience in site monitoring, clinical data management, or clinical operations.

• Ability to identify and interpret business trends and apply findings to centralized monitoring practices.

Required Technical Skills

• Programming: Python, R, SQL, or SAS.

• Data analytics: Clinical trial data analysis, reporting, and interpretation of KRIs and KPIs.

• RBQM systems: System configuration, implementation, execution, and troubleshooting.

• Database management: Database design, clinical databases, and system integration.

• Automation: Developing scripts to automate analytical workflows.

• Clinical research compliance: Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes.

• Communication: Ability to collaborate with cross-functional teams and present findings clearly.

• Problem-solving: Critical thinking, attention to detail, and troubleshooting data refreshes and execution errors.

Career Opportunity in Clinical Data Analytics

This position is suited to experienced professionals looking to advance their careers in centralized monitoring, clinical data surveillance, and risk-based quality management. It combines clinical research knowledge with programming, analytical problem-solving, and system configuration to support data-driven decisions throughout clinical trials.

How to Apply

Interested candidates can review the complete job description and apply through Parexel’s recruitment portal.

Apply here: Senior Data Surveillance Analyst – Parexel Official Careers

Candidates should verify the current application status and location-specific requirements on the official careers page before applying.

Job Summary

Stallion Laboratories Pvt. Ltd. is inviting applications for multiple positions in its Quality Control (QC) department within pharmaceutical formulations.
The available roles include Officer, Senior Officer, Executive, Assistant Manager, and Deputy Manager across different QC functions.
Candidates with 2–14 years of relevant experience can apply for positions involving analytical method validation, QC documentation, HPLC analysis, GC operations, GLP documentation, and raw material and finished product planning.
Interested candidates can submit their updated resumes to the recruitment email addresses provided below.

Company Overview

Stallion Laboratories Pvt. Ltd. operates in the pharmaceutical formulations sector and is seeking experienced professionals to strengthen its Quality Control team. The openings cover analytical testing, laboratory documentation, LIMS management, and QC planning activities.

Stallion Laboratories QC Department Vacancies

1. Officer / Senior Officer – AMV/AMT / QC Documentation

• Department: Quality Control (QC)
• Experience: 2–4 years
• Job Function: Analytical Method Validation (AMV), Analytical Method Transfer (AMT), and QC documentation.

2. Executive – GLP Documentation & LIMS Master

• Department: Quality Control (QC)
• Experience: 5–8 years
• Required Knowledge: Specifications (SPECs), Standard Testing Procedures (STPs), and Test Data Procedures (TDPs).
• Job Function: GLP documentation and LIMS master management.

3. Officer / Senior Officer – HPLC Analysis / GC Operations

• Department: Quality Control (QC)
• Experience: 2–4 years
• Job Function: HPLC analysis and gas chromatography (GC) operations.

4. Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning

• Department: Quality Control (QC)
• Experience: 10–14 years
• Job Function: Raw Material (RM), Packaging Material (PM), and Finished Goods/Finished Product (FG/FP) planning activities.

Eligibility & Qualifications

Educational Qualifications

Candidates with relevant educational qualifications for pharmaceutical Quality Control roles may apply. The recruitment announcement does not specify particular degrees or academic streams.

Experience Requirements

• Officer / Senior Officer – AMV/AMT / QC Documentation: 2–4 years.
• Executive – GLP Documentation & LIMS Master: 5–8 years.
• Officer / Senior Officer – HPLC Analysis / GC Operations: 2–4 years.
• Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning: 10–14 years.

Required Skills

• Knowledge of pharmaceutical Quality Control processes.
• Understanding of analytical method validation and method transfer.
• Familiarity with GLP documentation and LIMS master management.
• Knowledge of specifications, STPs, and TDPs.
• Experience in HPLC analysis and GC operations for relevant positions.
• Understanding of raw material, packaging material, and finished product planning for relevant managerial roles.
• Commitment to pharmaceutical quality standards and regulatory compliance.

Location & Salary

Job Location

The recruitment announcement does not specify the job location.

Salary Details

The salary package has not been disclosed. Compensation may vary depending on the position, relevant experience, and company policies.

 

How to Apply

Interested candidates can send their updated resumes to either of the following email addresses:

• Email: aarti.oberoi@stallionlabs.com
• Email: paresh.patel@stallionlabs.com

Application Instructions

1. Prepare an updated resume highlighting relevant pharmaceutical QC experience.
2. Mention the exact position applied for in the email subject line.
3. Send the application to one of the email addresses listed above.
4. Ensure your experience and technical skills match the requirements of the selected position.

Frequently Asked Questions

1. Which company is hiring for Quality Control jobs?

Stallion Laboratories Pvt. Ltd. is recruiting professionals for multiple Quality Control positions.

2. What positions are available?

The openings include Officer / Senior Officer – AMV/AMT / QC Documentation, Executive – GLP Documentation & LIMS Master, Officer / Senior Officer – HPLC Analysis / GC Operations, and Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning.

3. Can freshers apply for these vacancies?

The advertised positions require 2–14 years of experience. Freshers are not eligible based on the stated experience requirements.

4. What qualifications are required?

Specific educational qualifications have not been mentioned in the recruitment announcement. Candidates should have relevant qualifications and experience for their chosen QC role.

5. How can candidates apply?

Candidates can email their updated resumes to aarti.oberoi@stallionlabs.com or paresh.patel@stallionlabs.com. The position applied for should be mentioned in the email subject line.

6. What is the salary offered?

The salary details have not been disclosed in the recruitment announcement.

Job Summary

Category	Details
Company	Stallion Laboratories Pvt. Ltd.
Vacancies	Officer / Senior Officer – AMV/AMT / QC Documentation; Executive – GLP Documentation & LIMS Master; Officer / Senior Officer – HPLC Analysis / GC Operations; Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning
Required Education	Relevant qualifications for pharmaceutical Quality Control roles; specific degrees not stated
Experience	2–4 years, 5–8 years, 2–4 years, and 10–14 years, respectively

 

Novumgen is inviting applications for the position of Regulatory Affairs Executive – Mexico Market at its Vadodara, Gujarat location.
The opportunity is suitable for candidates with 1–4 years of experience in pharmaceutical regulatory affairs.
The role involves regulatory submissions to COFEPRIS, dossier preparation, product registrations, renewals, and regulatory lifecycle management.
Interested candidates with relevant regulatory affairs experience can send their updated CV to the recruitment email address provided below.

Company Overview

Novumgen is hiring a Regulatory Affairs Executive to support pharmaceutical regulatory activities for the Mexico market. The position involves coordinating regulatory submissions, maintaining product registration documentation, and working with cross-functional teams and external partners.

Novumgen Regulatory Affairs Executive Job Details

Position Information

• Department: Regulatory Affairs
• Designation: Regulatory Affairs Executive – Mexico Market
• Location: Vadodara, Gujarat
• Experience: 1–4 years

Job Role & Responsibilities

Key Responsibilities

• Prepare and coordinate regulatory submissions for pharmaceutical products to COFEPRIS, Mexico’s regulatory authority.
• Support dossier preparation for new product registrations, renewals, variations, and modifications.
• Provide regulatory support to cross-functional teams.
• Handle deficiency responses for Marketing Authorization Applications.
• Coordinate with partners to ensure the timely availability of required information.
• Ensure timely submission of variations and commercial urgency requests to regulatory authorities.
• Maintain regulatory project trackers and documentation.
• Manage renewals and other regulatory lifecycle activities.

Eligibility & Qualifications

Educational Qualifications

Candidates should have relevant qualifications for pharmaceutical regulatory affairs. The recruitment announcement does not specify a particular degree.

Experience Requirements

• 1–4 years of experience in pharmaceutical regulatory affairs.
• Familiarity with regulatory submissions and dossier preparation is relevant to the role.
• Experience with product registrations, renewals, variations, and regulatory documentation is beneficial.

Required Skills

• Regulatory submission coordination.
• Pharmaceutical dossier preparation and maintenance.
• Knowledge of Marketing Authorization Applications and deficiency responses.
• Regulatory project tracking and documentation management.
• Coordination with cross-functional teams and external partners.
• Ability to manage submission timelines and regulatory lifecycle activities.

Location & Salary

Job Location

Vadodara, Gujarat, India.

Salary Details

The salary package has not been specified in the recruitment announcement. Compensation may depend on the candidate’s qualifications, experience, and the company’s policies.

How to Apply

Interested candidates can share their updated CV through the recruitment email address below.

Email: tisha.thakkar@novumgen.com

Application Instructions

1. Prepare an updated CV highlighting relevant pharmaceutical regulatory affairs experience.
2. Include experience in regulatory submissions, dossier preparation, product registrations, renewals, and variations, where applicable.
3. Send your CV to tisha.thakkar@novumgen.com.

Frequently Asked Questions

1. Which company is hiring for the Regulatory Affairs Executive position?

Novumgen is recruiting for the Regulatory Affairs Executive – Mexico Market position.

2. What is the required experience?

Candidates should have 1–4 years of experience.

3. Where is the job located?

The position is based in Vadodara, Gujarat.

4. What are the main responsibilities?

The role includes COFEPRIS submissions, dossier preparation, registration renewals, variations, deficiency responses, and regulatory documentation management.

5. How can candidates apply?

Candidates can email their updated CV to tisha.thakkar@novumgen.com.

6. Is a specific educational qualification mentioned?

The recruitment announcement does not specify a particular degree. Candidates should have relevant qualifications and experience for the role.

Job Summary

Category	Details
Company	Novumgen
Vacancies	Regulatory Affairs Executive – Mexico Market
Required Education	Relevant qualification for pharmaceutical regulatory affairs
Experience	1–4 years
Location	Vadodara, Gujarat

Akums Drugs & Pharmaceuticals Ltd. is hiring an Assistant Research Associate for its Analytical Research & Development (ARD) department in Haridwar, Uttarakhand.
The opportunity is open to candidates with B.Pharm, M.Pharm, or M.Sc. in Chemistry qualifications.
Applicants should have 3–4 years of experience in analytical method development, validation, and method transfer.
Candidates with hands-on experience in HPLC, GC, dissolution testing, and other analytical instruments can submit their updated resumes for consideration.

Company Overview

Akums Drugs & Pharmaceuticals Ltd. is inviting experienced professionals to join its Analytical Research & Development (ARD) team. The advertised role focuses on analytical method development, validation, method transfer, and pharmaceutical product analysis.

Akums Drugs ARD Job Details

Assistant Research Associate – Analytical Research & Development

• Department: Analytical Research & Development (ARD)
• Designation: Assistant Research Associate
• Location: Haridwar, Uttarakhand
• Experience: 3–4 years
• Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry)

Job Role & Responsibilities

Key Responsibilities

• Perform analytical method development, validation, and method transfer activities.
• Operate HPLC, GC, dissolution testing equipment, UV-Visible spectrophotometers, FTIR, and other analytical instruments.
• Work on HPLC column selection, buffer optimization, assay, dissolution, related substances (RS), and organic volatile impurity (OVI) methods.
• Follow applicable FDA, ICH, USP, IP, BP, and JP guidelines.
• Analyse raw materials, stability samples, trial batches, and finished products.
• Support the preparation of STS/STP, COA, and AMV protocols.

Eligibility & Qualifications

Educational Qualifications

• B.Pharm
• M.Pharm
• M.Sc. in Chemistry

Experience Requirements

• 3–4 years of relevant experience in Analytical Research & Development.
• Experience in analytical method development, validation, and method transfer.
• Hands-on experience with HPLC, GC, dissolution, UV-Visible spectrophotometry, and FTIR.

Required Skills

• Knowledge of HPLC column selection and buffer optimization.
• Understanding of assay, dissolution, RS, and OVI methods.
• Familiarity with FDA, ICH, USP, IP, BP, and JP guidelines.
• Experience analysing pharmaceutical raw materials, stability samples, trial batches, and finished products.
• Knowledge of preparing STS/STP, COA, and AMV protocols.

Location & Salary

Job Location

Haridwar, Uttarakhand, India.

Salary Details

The salary package has not been specified in the recruitment announcement. Compensation may depend on qualifications, relevant experience, and the company’s policies.

How to Apply

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

Email: hr.pch@akums.in

Application Instructions

1. Prepare an updated resume with your educational qualifications and relevant ARD experience.
2. Highlight your experience in analytical method development, validation, method transfer, and analytical instrumentation.
3. Include relevant experience with pharmaceutical testing methods and regulatory guidelines.
4. Send your resume to hr.pch@akums.in.

Frequently Asked Questions

1. Which company is hiring for the Assistant Research Associate – ARD position?

Akums Drugs & Pharmaceuticals Ltd. is recruiting for its Analytical Research & Development department.

2. What qualifications are required?

Candidates with B.Pharm, M.Pharm, or M.Sc. in Chemistry can apply.

3. How much experience is required?

The position requires 3–4 years of relevant experience.

4. Which technical skills are required?

Candidates should have experience in analytical method development, validation, method transfer, HPLC, GC, dissolution, UV-Visible spectrophotometry, and FTIR.

5. Where is the job located?

The position is based in Haridwar, Uttarakhand.

6. How can candidates apply?

Candidates can email their updated resumes to hr.pch@akums.in.

Job Summary

Category	Details
Company	Akums Drugs & Pharmaceuticals Ltd.
Vacancies	Assistant Research Associate – Analytical Research & Development
Required Education	B.Pharm, M.Pharm, M.Sc. (Chemistry)
Experience	3–4 years
Location	Haridwar, Uttarakhand

Ajanta Pharma is inviting applications for Quality Assurance (QA) positions at its US FDA formulation plant in Paithan, Chhatrapati Sambhajinagar, Maharashtra.
The recruitment is open to candidates with B.Pharm, M.Pharm, B.Sc., or M.Sc. qualifications, depending on the position.
Applicants should have 3–5 years of relevant experience in pharmaceutical manufacturing, quality systems, qualification, or validation activities.
Interested candidates can send their updated resumes to the recruitment email address provided by the company.

Company Overview

Ajanta Pharma is a pharmaceutical company with formulation manufacturing operations. The company is seeking QA professionals for its US FDA formulation plant in Paithan, Maharashtra.

Ajanta Pharma Quality Assurance Job Vacancies

1. QA Position for B.Pharm / M.Pharm Candidates

Department: Quality Assurance (QA)

Qualification: B.Pharm / M.Pharm

Experience: 3–5 years

Job Role & Responsibilities

• Experience working in an OSD formulation plant operating under regulated requirements.
• Knowledge of Quality Management Systems (QMS), change control, CAPA, deviations, and market complaints.
• Experience using relevant software systems, including QMS, TrackWise, and E-log systems.

2. QA Position for B.Sc. / M.Sc. Candidates

Department: Quality Assurance (QA)

Qualification: B.Sc. / M.Sc.

Experience: 3–5 years

Job Role & Responsibilities

• Prepare and review qualification and requalification protocols and reports.
• Execute qualification and validation studies.
• Review analytical reports.
• Understand various laboratory instruments and analytical testing methods.

Eligibility & Qualifications

Educational Qualifications

• B.Pharm
• M.Pharm
• B.Sc.
• M.Sc.

Candidates should select the position that matches their educational background and relevant experience.

Experience Requirements

• QA, B.Pharm / M.Pharm: 3–5 years.
• QA, B.Sc. / M.Sc.: 3–5 years.

Required Skills

• Knowledge of pharmaceutical quality assurance practices.
• Understanding of QMS, change control, CAPA, and deviation management.
• Familiarity with TrackWise and E-log systems, where applicable.
• Experience in qualification and requalification documentation.
• Knowledge of validation studies, analytical reports, laboratory instruments, and analytical testing methods.

Location & Salary

Job Location

Ajanta Pharma Ltd.

B-4/5/6 MIDC Area, Paithan, District Chhatrapati Sambhajinagar, Maharashtra – 431148.

Salary Details

The salary package has not been specified in the recruitment announcement. Compensation may depend on the candidate’s qualifications, experience, and relevant skills.

How to Apply

Interested candidates can submit their updated resumes by email.

Email: cv.ptn@ajantapharma.com

Application Instructions

1. Prepare an updated resume highlighting your qualifications and relevant QA experience.
2. Include experience in pharmaceutical manufacturing, QMS, qualification, validation, or analytical testing, as applicable.
3. Send your resume to the recruitment email address provided above.

Application validity: The recruitment announcement states that the communication is valid until 30 October 2026.

Frequently Asked Questions

1. Which company is hiring for QA positions?

Ajanta Pharma is recruiting candidates for Quality Assurance positions at its Paithan formulation plant.

2. What qualifications are accepted?

The listed qualifications are B.Pharm, M.Pharm, B.Sc., and M.Sc., depending on the position.

3. How much experience is required?

Both advertised QA positions require 3–5 years of relevant experience.

4. What skills are required for these positions?

Candidates may need experience in QMS, change control, CAPA, deviations, qualification, validation, analytical reports, and laboratory testing methods, depending on the role.

5. How can candidates apply?

Candidates can email their updated resumes to cv.ptn@ajantapharma.com.

6. What is the application validity date?

The recruitment announcement states that the communication is valid until 30 October 2026.

Job Summary

Category	Details
Company	Ajanta Pharma Ltd.
Vacancies	Quality Assurance (QA) positions for B.Pharm / M.Pharm and B.Sc. / M.Sc. candidates
Required Education	B.Pharm, M.Pharm, B.Sc., M.Sc.
Experience	3–5 years for both positions
Location	Paithan, Chhatrapati Sambhajinagar, Maharashtra

Cipla is conducting a walk-in interview for Jr. Operator, Sr. Officer, and Apprentice positions at its facility in Verna, Goa.
The recruitment drive covers OSD manufacturing and packing, MDI filling, sterile aseptic filling, and maintenance and electrical engineering operations.
Candidates with a Diploma in Pharmacy, B.Sc., Diploma in Mechanical or Electrical Engineering, or B.E./B.Tech in Mechanical or Electrical Engineering can apply according to the role.
Freshers are eligible for the Apprentice position, while experienced candidates can apply for the other openings based on the specified experience requirements.

Cipla Company Overview

Cipla is a pharmaceutical company involved in the development and manufacturing of medicines. The company is inviting applications for manufacturing, packing, engineering, and apprenticeship roles at its Verna facility in Goa.

Cipla Walk-In Interview Details

• Interview Date: 18 October 2026 (Sunday)
• Interview Time: 9:00 AM to 4:00 PM
• Job Location: Goa
• Interview Venue: Cipla Academy, Cipla Ltd., Verna Industrial Estate, Verna, Goa – 403722

Cipla Job Vacancies and Responsibilities

Jr. Operator Jobs at Cipla

Experience: 1–4 years

Educational Qualifications:

• Diploma in Pharmacy
• B.Sc.
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering

Job Role & Responsibilities

The Jr. Operator position includes the following manufacturing and packing operations:

• Oral Solid Dosage (OSD) manufacturing and packing.
• Granulation and compression.
• Coating operations.
• Primary and secondary packing.
• Bottle packing.
• Metered Dose Inhaler (MDI) filling operations.
• Sterile aseptic filling operations.

Candidates should have relevant experience in pharmaceutical manufacturing operations.

Sr. Officer Jobs at Cipla

Experience: 4–8 years

Educational Qualifications:

• B.E. in Mechanical Engineering
• B.Tech in Mechanical Engineering
• B.E. in Electrical Engineering
• B.Tech in Electrical Engineering

Job Role & Responsibilities

• Handle maintenance and electrical engineering operations.
• Support engineering activities in pharmaceutical manufacturing.
• Apply relevant mechanical or electrical engineering knowledge to manufacturing facility operations.

Candidates should have experience in pharmaceutical manufacturing and an electrical or mechanical engineering background.

Apprentice Jobs at Cipla

Experience: Freshers

Educational Qualifications:

• Diploma in Pharmacy
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering

Job Role & Responsibilities

• Assist with OSD manufacturing operations.
• Support MDI manufacturing operations.
• Assist with sterile manufacturing activities under supervision.

This position provides an opportunity for freshers to gain practical exposure to pharmaceutical manufacturing operations.

Eligibility & Qualifications

Candidates should meet the educational and experience requirements for their preferred position.

Educational Qualifications

• Diploma in Pharmacy
• B.Sc.
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering
• B.E. in Mechanical Engineering
• B.Tech in Mechanical Engineering
• B.E. in Electrical Engineering
• B.Tech in Electrical Engineering

Experience Requirements

• Jr. Operator: 1–4 years
• Sr. Officer: 4–8 years
• Apprentice: Freshers

Additional Requirements

• Candidates residing in Goa will be given preference.
• Applicants for experienced positions must have relevant pharmaceutical manufacturing experience.
• Candidates should have experience in facilities approved by regulatory authorities such as USFDA, MHRA, EU-GMP, or other recognized agencies, as applicable to the role.

Location & Salary

Job Location

Cipla Ltd., Verna Industrial Estate, Verna, Goa – 403722.

Salary Details

The salary package has not been specified in the recruitment notice. Compensation and other employment terms may vary according to the position and the company’s policies.

How to Apply

Interested candidates should attend the walk-in interview at the venue mentioned below.

Interview Date: 18 October 2026
Interview Time: 9:00 AM to 4:00 PM
Venue: Cipla Academy, Cipla Ltd., Verna Industrial Estate, Verna, Goa – 403722.

Application Instructions

• Review the eligibility criteria before attending the interview.
• Carry an updated resume and relevant educational and experience documents.
• Candidates should be prepared to undergo the company’s evaluation process.
• Scan the QR code provided in the recruitment poster to access the application process.

Important Instructions

• Preference will be given to candidates who are residents of Goa.
• Cipla reserves the right to conduct an evaluation process.
• CV shortlisting will be carried out according to the company’s terms and conditions.
• Candidates applying for experienced positions must have relevant pharmaceutical manufacturing experience in facilities approved by recognized regulatory authorities.

Frequently Asked Questions

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

Cipla is conducting the walk-in interview for manufacturing, engineering, and apprenticeship positions.

2. Which positions are available?

The openings include Jr. Operator, Sr. Officer, and Apprentice.

3. Are freshers eligible to apply?

Yes. Freshers can apply for the Apprentice position.

4. What qualifications are required?

The listed qualifications include Diploma in Pharmacy, B.Sc., Diploma in Mechanical or Electrical Engineering, and B.E./B.Tech in Mechanical or Electrical Engineering, depending on the role.

5. When and where is the interview?

The walk-in interview is scheduled for 18 October 2026, from 9:00 AM to 4:00 PM, at Cipla Academy, Verna Industrial Estate, Verna, Goa – 403722.

6. What experience is required?

Jr. Operator candidates need 1–4 years of experience, Sr. Officer candidates need 4–8 years, and freshers can apply for the Apprentice position.

Job Summary

Category	Details
Company	Cipla
Vacancies	Jr. Operator, Sr. Officer, Apprentice
Required Education	Diploma in Pharmacy, B.Sc., Diploma in Mechanical/Electrical Engineering, B.E./B.Tech in Mechanical/Electrical Engineering
Experience	Jr. Operator: 1–4 years; Sr. Officer: 4–8 years; Apprentice: Freshers
Location	Verna Industrial Estate, Verna, Goa

Glenmark Pharmaceuticals Ltd is inviting applications for multiple positions at its Nashik facility.
The current openings include Officer (Engineering), Executive and Jr Officer (Warehouse), Sr. Officer (QC), and Executive (QC).
Candidates with B.E. (Mechanical), D.M.E., D. Pharmacy, B.Sc., or M.Sc. qualifications can apply according to the requirements of each position.
Interested candidates can submit their updated CV by email for consideration.

Company Overview

Glenmark Pharmaceuticals Ltd is a pharmaceutical company involved in medicine manufacturing and formulations for domestic and international markets. The company is seeking candidates for engineering, warehouse, and quality control roles at its Nashik location.

Glenmark Pharmaceuticals Engineering Jobs

Officer (Engineering)

Qualification: B.E. (Mechanical) / D.M.E.

Experience: 2–4 years

Job Role & Responsibilities

• Pharmaceutical machine maintenance.
• AutoCAD-related work.
• Supporting engineering and maintenance activities in a pharmaceutical manufacturing environment.

Glenmark Pharmaceuticals Warehouse Jobs

Executive & Jr Officer (Warehouse)

Qualification: D. Pharmacy / B.Sc.

Experience: 2–4 years in the pharmaceutical industry.

Job Role & Responsibilities

• Support warehouse operations in a pharmaceutical manufacturing facility.
• Perform duties associated with the assigned warehouse position.

Glenmark Pharmaceuticals Quality Control Jobs

Sr. Officer (QC)

Qualification: M.Sc. / B.Sc.

Experience: 5–10 years

Job Role & Responsibilities

• Instrument handling.
• Quality Management System (QMS) activities.
• Analysis and QC validation.

Executive (QC)

Qualification: M.Sc. / B.Sc.

Experience: 10–15 years

Job Role & Responsibilities

• Handle QMS activities.
• Manage change control (CC) and deviation-related activities.
• Support out-of-specification (OOS) and out-of-trend (OOT) investigations.
• Perform root cause analysis and corrective and preventive action (CAPA) activities.
• Handle instruments used in quality control operations.

Eligibility & Qualifications

Candidates should have the qualifications and experience relevant to their preferred position.

Educational Qualifications

• Engineering: B.E. (Mechanical) / D.M.E.
• Warehouse: D. Pharmacy / B.Sc.
• Quality Control: M.Sc. / B.Sc.

Experience Requirements

• Officer (Engineering): 2–4 years in pharmaceutical machine maintenance and AutoCAD.
• Executive / Jr Officer (Warehouse): 2–4 years in the pharmaceutical industry.
• Sr. Officer (QC): 5–10 years in instrument handling, QMS, analysis, and QC validation.
• Executive (QC): 10–15 years in QMS activities, change control, deviations, OOS/OOT, root cause analysis, CAPA, and instrument handling.

Location & Salary

Job Location

Nashik, Maharashtra, India.

Salary Details

The salary package has not been specified in the recruitment announcement. Compensation may vary according to the position, qualifications, and relevant experience.

How to Apply

Interested candidates should send their updated CV to the recruitment contact below.

Email: Shreya.tiwari@glenmarkpharma.com

LinkedIn: https://www.linkedin.com/in/shreya-tiwari-719266206

Application Instructions

• Prepare an updated CV with your educational qualifications and work experience.
• Mention the position you are applying for in your email.
• Include relevant details of pharmaceutical machine maintenance, warehouse operations, or QC experience, as applicable.

Important Recruitment Notice

Glenmark states that it does not collect recruitment fees or charges, or any other valuables, as a pre-employment or post-employment requirement. Candidates should be cautious of requests for money during the recruitment process.

Frequently Asked Questions

1. Which company is hiring?

Glenmark Pharmaceuticals Ltd is hiring for engineering, warehouse, and quality control positions.

2. Which positions are available?

The advertised positions are Officer (Engineering), Executive and Jr Officer (Warehouse), Sr. Officer (QC), and Executive (QC).

3. What qualifications are required?

B.E. (Mechanical), D.M.E., D. Pharmacy, B.Sc., and M.Sc. are listed for the respective positions.

4. How much experience is required?

The experience requirements range from 2–4 years for engineering and warehouse roles to 5–15 years for the listed QC positions.

5. How can candidates apply?

Candidates can email their updated CV to Shreya.tiwari@glenmarkpharma.com.

6. Does Glenmark charge recruitment fees?

No. The recruitment notice states that Glenmark does not collect recruitment fees or charges from candidates.

Job Summary

Category	Details
Company	Glenmark Pharmaceuticals Ltd
Vacancies	Officer (Engineering); Executive / Jr Officer (Warehouse); Sr. Officer (QC); Executive (QC)
Required Education	B.E. (Mechanical), D.M.E., D. Pharmacy, B.Sc., M.Sc.
Experience	Engineering: 2–4 years; Warehouse: 2–4 years; Sr. Officer (QC): 5–10 years; Executive (QC): 10–15 years
Location	Nashik, Maharashtra

Tashi Pharma is hiring two candidates for the position of Regulatory Affairs Executive in Ahmedabad, Gujarat.
The opportunity is open to freshers and experienced professionals interested in pharmaceutical regulatory affairs and product registration.
Candidates with a B.Pharm, M.Pharm, or a relevant life sciences qualification can apply, with prior regulatory affairs experience preferred.
Interested applicants can send their updated resumes to the company’s recruitment email address.

Company Overview

Tashi Pharma is inviting applications for its Regulatory Affairs department. The role involves preparing pharmaceutical registration dossiers, maintaining regulatory documentation, coordinating with internal departments, and supporting product registrations across international markets.

Tashi Pharma Regulatory Affairs Executive Job Details

Position Information

• Company: Tashi Pharma
• Department: Regulatory Affairs
• Designation: Regulatory Affairs Executive
• Number of Openings: 2
• Job Location: Ahmedabad, Gujarat
• Experience: Freshers and experienced candidates can apply

Job Role & Responsibilities

The selected candidates will support pharmaceutical regulatory documentation, dossier preparation, and registration activities.

Key Responsibilities

1. Prepare, compile, and review pharmaceutical registration dossiers in CTD and ACTD formats, as applicable.
2. Prepare and maintain regulatory dossiers and supporting documents for LATAM, Southeast Asian, and Rest of World (ROW) markets.
3. Coordinate the collection of technical documents from Quality Assurance (QA), Quality Control (QC), Manufacturing, and other internal departments.
4. Compile and maintain product specifications, Certificates of Analysis (CoAs), manufacturing details, stability data, analytical methods, GMP certificates, and other regulatory documents.
5. Prepare and manage country-specific regulatory documentation, application forms, declarations, undertakings, and supporting documents required for product registration.
6. Review dossiers for completeness, accuracy, consistency, and compliance with applicable regulatory guidelines and market-specific requirements.
7. Assist with the legalization, notarization, apostille, and certification of regulatory documents wherever required.
8. Monitor changes in country-specific regulatory requirements and communicate their potential impact to the team.

Eligibility & Qualifications

Educational Qualifications

• B.Pharm is preferred.
• M.Pharm is also relevant.
• Candidates with other relevant life sciences qualifications may be considered.

Experience Requirements

• Freshers can apply.
• Experienced candidates with pharmaceutical regulatory affairs experience will be preferred.
• Experience in export markets and pharmaceutical registration activities is an advantage.

Required Skills

• Knowledge of CTD and ACTD dossier preparation.
• Understanding of pharmaceutical registration documentation.
• Familiarity with GMP certificates, CoAs, product specifications, stability data, and manufacturing documentation.
• Good written and verbal communication skills.
• Strong organizational skills and attention to detail.
• Ability to manage multiple regulatory dossiers and deadlines.
• Proficiency in Microsoft Office, particularly Word and Excel.

Location & Salary

Job Location

Ahmedabad, Gujarat, India.

Salary Details

The salary package has not been specified in the recruitment announcement. Compensation may depend on the candidate’s qualifications, skills, and relevant experience.

How to Apply

Interested candidates can apply for the Regulatory Affairs Executive position by emailing their updated resume to the recruitment team.

Email: hr@tashipharma.com

Application Instructions

• Prepare an updated resume highlighting relevant pharmaceutical or life sciences qualifications.
• Include any experience in regulatory affairs, CTD/ACTD dossiers, pharmaceutical documentation, or product registration.
• Send the resume to the recruitment email address provided above.

Important Details

• A total of two vacancies are available.
• Both freshers and experienced candidates are eligible to apply.
• Candidates with pharmaceutical regulatory affairs experience, particularly in export markets, will be preferred.
• Knowledge of regulatory documentation and Microsoft Office is relevant to the role.

Frequently Asked Questions

1. What is the designation offered at Tashi Pharma?

The advertised position is Regulatory Affairs Executive.

2. How many vacancies are available?

There are two openings for the Regulatory Affairs Executive position.

3. Are freshers eligible to apply?

Yes. Freshers can apply, although candidates with prior pharmaceutical regulatory affairs experience will be preferred.

4. What qualifications are required?

B.Pharm is preferred. M.Pharm and relevant life sciences qualifications may also be considered.

5. Where is the job located?

The position is based in Ahmedabad, Gujarat.

6. How can candidates apply?

Candidates can email their updated resumes to hr@tashipharma.com.

Job Summary

Category	Details
Company	Tashi Pharma
Vacancies	Regulatory Affairs Executive: 2 openings
Required Education	B.Pharm preferred; M.Pharm or relevant life sciences qualification
Experience	Freshers and experienced candidates
Location	Ahmedabad, Gujarat

Ipca Laboratories Limited is inviting applications for multiple positions at its manufacturing facility in Pologround, Indore, Madhya Pradesh.
The recruitment drive includes openings in Production, PPA (API), Quality Assurance (API), and Quality Control departments.
Candidates with 12th, ITI, Diploma, undergraduate, or postgraduate qualifications in relevant fields can apply according to the position and experience requirements.
Interested candidates can send their updated resume to the recruitment email address, mentioning the applied position in the subject line.

Company Overview

Ipca Laboratories Limited is recruiting professionals for its pharmaceutical manufacturing operations in Pologround, Indore. The advertised positions cover production operations, API powder processing, quality assurance, and laboratory quality control.

Ipca Laboratories Production Jobs in Indore

Position Details

• Department: Production
• Designation: Technician / Chemist
• Qualification: 12th / ITI / Diploma / UG / PG in a relevant field
• Experience: Minimum 2 years

Job Role & Responsibilities

• Handle shift operations, batch charging, and production documentation.
• Operate equipment such as reactors, centrifuges, ANFDs, and RCVDs.
• Monitor batch production and ensure that operations follow approved SOPs and BPCRs.
• Check equipment, materials, utilities, and production documentation.
• Follow applicable safety and compliance requirements.

Ipca Laboratories PPA (API) Jobs in Indore

Position Details

• Department: PPA (API)
• Designation: Chemist / Officer
• Qualification: Undergraduate or postgraduate qualification in a relevant field
• Experience: 2–4 years

Job Role & Responsibilities

• Operate, monitor, and maintain powder-processing equipment.
• Handle filtration, drying, weighing, and packing activities.
• Complete production documentation according to approved SOPs and BPCRs.
• Follow applicable operating procedures and manufacturing requirements.

Ipca Laboratories Quality Assurance Jobs in Indore

Position Details

• Department: Quality Assurance (API)
• Designation: Assistant Manager
• Qualification: Undergraduate or postgraduate qualification in a relevant field
• Experience: Minimum 10–15 years

Job Role & Responsibilities

• Handle Annual Product Quality Review (APQR) activities.
• Manage QA SOPs and self-inspection activities.
• Support equipment qualification, process validation, and cleaning validation.
• Conduct quality risk assessments and support the Quality Management System (QMS).
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results.
• Handle market complaint investigations.

Ipca Laboratories Quality Control Jobs in Indore

Position Details

• Department: Quality Control
• Designation: Chemist
• Qualification: Undergraduate or postgraduate qualification in a relevant field
• Experience: Minimum 2 years

Job Role & Responsibilities

• Perform finished product, stability, and raw material analysis.
• Conduct particle size analysis and water testing.
• Perform instrument calibration.
• Handle LIMS and OneLab laboratory software.
• Support OOS/OOT analysis and method verification.
• Perform solution preparation and maintain laboratory documentation.
• Follow SOPs and maintain laboratory cleanliness.

Eligibility & Qualifications

Candidates should meet the educational and experience requirements specified for their preferred position.

Educational Qualifications

• 12th
• ITI
• Diploma
• Undergraduate qualification in a relevant field
• Postgraduate qualification in a relevant field

Experience Requirements

• Production Technician / Chemist: Minimum 2 years.
• PPA (API) Chemist / Officer: 2–4 years.
• Quality Assurance (API) Assistant Manager: Minimum 10–15 years.
• Quality Control Chemist: Minimum 2 years.

Additional Skills

• Knowledge of pharmaceutical manufacturing operations.
• Familiarity with SOPs and batch production documentation.
• Experience operating relevant API manufacturing equipment, where applicable.
• Knowledge of quality assurance procedures, validation, and investigations for QA roles.
• Experience in analytical testing, instrument calibration, and laboratory documentation for QC roles.

Location & Salary

Job Location

Ipca Laboratories Limited

Pologround, Indore, Madhya Pradesh, India.

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 send their updated resume to the recruitment email address below.

Email: abhishek.parmar@ipca.com

Contact Number: 7880147807

Application Instructions

• Send your updated resume to the specified email address.
• Mention the applied position in the subject line of your email.
• Include relevant qualifications, work experience, and technical skills in your resume.

Important Instructions

• Ipca Laboratories Limited states that it does not charge candidates recruitment fees at any stage of the hiring process.
• Do not make payments to individuals or agencies claiming to represent the company.
• Report suspicious recruitment-related payment requests to ipca@ipca.com or corporate.communication@ipca.com.

Frequently Asked Questions

1. Which company is hiring?

Ipca Laboratories Limited is recruiting for its manufacturing operations in Pologround, Indore.

2. Which departments have vacancies?

The openings are in Production, PPA (API), Quality Assurance (API), and Quality Control.

3. What qualifications are required?

The recruitment notice lists 12th, ITI, Diploma, and undergraduate or postgraduate qualifications in relevant fields, depending on the position.

4. How much experience is required?

The experience requirements range from a minimum of 2 years for Production and QC roles to 10–15 years for the Quality Assurance Assistant Manager position. PPA roles require 2–4 years.

5. How can candidates apply?

Candidates can email their updated resume to abhishek.parmar@ipca.com and mention the applied position in the email subject line.

6. Does Ipca Laboratories charge recruitment fees?

No. The recruitment notice states that the company does not charge candidates any recruitment fees.

Job Summary

Category	Details
Company	Ipca Laboratories Limited
Vacancies	Production Technician / Chemist, PPA Chemist / Officer, QA Assistant Manager, QC Chemist
Required Education	12th, ITI, Diploma, undergraduate or postgraduate qualification in a relevant field
Experience	Production: Minimum 2 years; PPA: 2–4 years; QA: Minimum 10–15 years; QC: Minimum 2 years
Location	Pologround, Indore, Madhya Pradesh