Ayur.AI Recruitment – Clinical Research Associate, Chennai

Ayur.AI is hiring a Clinical Research Associate for its clinical research team in Chennai, Tamil Nadu. This opportunity is suitable for candidates with a background in Life Sciences, Medicine, Nursing, Public Health, or related healthcare disciplines. The role involves coordinating clinical trial participants, managing study data, supporting biospecimen logistics, and maintaining research documentation in line with Good Clinical Practice (GCP) and Institutional Review Board (IRB) protocols. Candidates with 1–2 years of experience in clinical research or healthcare are encouraged to review the opportunity.

Company Overview

Ayur.AI focuses on personalized health and wellness through AI-powered Ayurveda solutions. Its platform offers personalized programs addressing metabolic health, gut health, and women’s health.

The company is also developing Integrative Diabetes Centers that combine Ayurveda, modern science, technology, and personalized health insights to address diabetes.

Job Details

Job Role & Responsibilities

The selected candidate will support the daily operations of longitudinal clinical trials involving Continuous Glucose Monitoring (CGM), laboratory testing, gut microbiome analysis, and remote physician consultations.

Participant Coordination

• Schedule and follow up on appointments for CGM setup, laboratory tests, stool sample collection, and virtual consultations.

• Provide participants with clear instructions on app usage and study-related test procedures.

Data Collection & Management

• Monitor and collect data from wearable CGM devices and study-related applications.

• Enter and validate participant data in study databases and Case Report Forms (CRFs) within the required timelines.

• Identify and report data inconsistencies or protocol deviations to the study coordinator or Principal Investigator (PI).

Communication & Support

• Coordinate communication between participants, clinical laboratories, logistics partners, physicians, and the internal research team.

• Maintain regular and empathetic communication with participants to encourage study adherence and address concerns.

• Coordinate specimen shipment and tracking with third-party laboratories.

Documentation & Compliance

• Maintain accurate participant records in accordance with Good Clinical Practice (GCP) and IRB protocols.

• Maintain participant information sheets, informed consent forms, and data-tracking documents.

Eligibility & Qualifications

Candidates should have a bachelor’s degree in a health-related discipline, such as Life Sciences, Medicine, Nursing, Public Health, or a similar field.

Relevant courses may include B.Sc. Life Sciences, M.Sc. Life Sciences, B.Pharm, M.Pharm, Pharm.D, B.Sc. Nursing, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Microbiology, M.Sc. Microbiology, or Public Health qualifications, where relevant to the employer’s health-related qualification requirement.

Experience Requirements

• Experience in a clinical research or healthcare setting is preferred.

• Relevant internships may also be considered.

• Knowledge of laboratory logistics and biospecimen handling is beneficial.

• Familiarity with Continuous Glucose Monitoring (CGM) devices and mobile health-tracking tools is an advantage.

Required Skills

• Proficiency in spreadsheets, including Microsoft Excel or Google Sheets.

• Familiarity with electronic data capture (EDC) platforms or research data management systems.

• Strong organizational skills and attention to detail.

• Excellent verbal and written communication skills.

• Ability to work independently, manage time efficiently, and handle multiple tasks.

• Ability to communicate with patients remotely and explain technical procedures in simple language.

• Empathetic, proactive, and collaborative approach to participant support.

 

How to Apply

Interested candidates can review the job listing and apply through LinkedIn.

Apply here: Clinical Research Associate – Ayur.AI

Applicants should review the official listing for the latest application status and any additional employer requirements.

Job Summary

GSK Recruitment 2026 – Senior Regulatory Specialist

GSK is inviting applications for the Senior Regulatory Specialist position in Bengaluru, India. This opportunity is suited to professionals with experience in pharmaceutical regulatory affairs, Chemistry, Pharmacy, or related scientific disciplines. The role focuses on Chemistry, Manufacturing and Controls (CMC) regulatory submissions, global dossier strategy, and regulatory compliance across multiple vaccine projects. Candidates with 3–8 years of experience and knowledge of global regulatory requirements may be suitable for this opportunity.

Company Overview

GSK is a global biopharmaceutical company focused on developing medicines and vaccines to prevent and treat diseases. Its research and development activities span respiratory diseases, immunology and inflammation, oncology, HIV, and infectious diseases.

The company brings together science, technology, and talent to advance drug development and improve patient health worldwide.

Job Details

Job Role & Responsibilities

The Senior Regulatory Specialist will represent the CMC Delivery team on regulatory networks and matrix teams, supporting Pharma Supply Chain, Commercial, Quality Assurance, third-party Contract Manufacturing Organizations, and the Office of the Chief Medical Officer in preparing components for global regulatory dossiers.

Key responsibilities include:

• Independently manage multiple vaccine CMC regulatory submission assignments across different dosage forms.

• Execute agreed dossier strategies and ensure regulatory submissions meet their intended requirements.

• Assess data and documentation to confirm that regulatory dossiers are fit for purpose.

• Identify risks associated with submission data and information packages.

• Escalate issues with potential business impact to the line manager.

• Review and approve dossiers prepared by peers, where required.

• Identify opportunities to improve regulatory processes, policies, and systems.

• Interpret regulations, guidelines, procedures, and policies related to pharmaceutical product registration and manufacturing.

• Support the submission, review, and approval of global regulatory applications.

• Provide subject matter expertise and regulatory guidance within the department and to external stakeholders.

• Mentor and train new team members.

• Build effective working relationships with relevant stakeholders, including Pharma Supply Chain, Local Operating Companies, and other project teams.

• Communicate project and policy matters across GSK to support appropriate regulatory and business decisions.

Eligibility & Qualifications

Candidates should have a bachelor’s degree in Chemistry, Pharmacy, or another related scientific or technical discipline.

Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Chemistry, M.Sc. Chemistry, B.Sc. Pharmaceutical Sciences, M.Sc. Pharmaceutical Sciences, or other related scientific or technical qualifications. The official posting specifies the relevant degree disciplines rather than an exhaustive list of accepted courses.

Experience Requirements

• 3–8 years of experience in a relevant regulatory or scientific environment, as stated in the posting.

• Experience working in a complex scientific organization.

• Knowledge of global or EMAP regulatory submissions.

• Understanding of regulatory agency guidelines and submission requirements.

• Broad understanding of the pharmaceutical industry, drug development, and research and development processes.

• Ability to interpret and advise on global regulatory guidelines and requirements.

Required Skills

Applicants should demonstrate the following capabilities:

• Strong organizational skills and attention to detail.

• Commitment to delivering high-quality work under regulatory submission deadlines.

• Excellent written and verbal communication skills.

• Ability to present regulatory information clearly and concisely.

• Understanding of the regulatory environment and pharmaceutical manufacturing requirements.

• Ability to manage multiple assignments and changing priorities.

• Strong stakeholder management and collaboration skills.

• Ability to work effectively in a matrix organization.

• Flexibility in responding to shifting project timelines and business requirements.

• Ability to provide regulatory guidance and share knowledge with colleagues.

Work Location & Arrangement

The position is based in Bengaluru, India. The job details identify the arrangement as hybrid, while the work arrangement description states that the role is on-site in India and involves collaboration with local and global colleagues, including virtual meetings. Candidates should check the official listing for the applicable work arrangement.

Salary & Benefits

The job posting includes a salary range of PLN 144,750 to PLN 241,250 as a location-specific pay-transparency disclosure. This is a Polish złoty salary range and should not be interpreted as the salary offered for the Bengaluru position.

 

How to Apply

Interested candidates can review the full job description and submit their applications through GSK’s official careers website.

Apply here: GSK Senior Regulatory Specialist – Official Careers Page

GSK does not charge any recruitment fee. Applicants should avoid paying individuals or agencies for job applications, interviews, or recruitment opportunities.

Job Summary

Thermo Fisher Scientific Recruitment – Centralized Monitoring Analyst (Level I & II)

Thermo Fisher Scientific is hiring for the Centralized Monitoring Analyst (Level I & II) position within its clinical research services team. This opportunity is associated with the company’s PPD clinical research portfolio and focuses on reviewing clinical trial data, identifying trends, and supporting risk-based centralized monitoring activities. Candidates with experience in clinical monitoring, clinical data management, biostatistics, or related clinical trial functions may be suitable for this role. Applicants should have a relevant degree or equivalent qualification and approximately two or more years of comparable experience.

Company Overview

Thermo Fisher Scientific provides scientific services and solutions, including clinical research services through its PPD clinical research business. The clinical research team supports the development of medicines and therapies by helping pharmaceutical and biotechnology companies conduct clinical trials.

Job Details

Job Role & Responsibilities

The Centralized Monitoring Analyst reviews clinical trial data and identifies issues, trends, signals, and potential risks that may require follow-up by project teams.

Key responsibilities include:

• Review clinical trial data using various tools and systems in accordance with the centralized monitoring plan, with support from senior team members.

• Characterize and track evidence of issues, signals, and potential risks.

• Ensure that review results are documented appropriately according to departmental procedures.

• Participate in the development of risk characterization and reporting, where required.

• Support review setup activities, including updating departmental databases and generating reports.

• Analyze operational and patient clinical trial data to identify trends and potential concerns.

• Communicate identified issues and potential risks to project team members for follow-up action.

Eligibility & Qualifications

Candidates should meet the following educational requirements:

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. Microbiology, M.Sc. Microbiology, Statistics, Biostatistics, or related clinical research qualifications. These are examples of potentially relevant courses; the official posting specifies a bachelor’s degree or equivalent qualification rather than an exhaustive list of accepted degrees.

• Bachelor’s degree or equivalent, along with a relevant formal academic or vocational qualification.

• Previous experience providing the knowledge, skills, and abilities required for the role, comparable to 2+ years.

• Prior experience in clinical monitoring, data management, biostatistics, or a related field supporting clinical trials is preferred.

An equivalent combination of appropriate education, training, and directly related experience may also be considered.

Knowledge & Skills Required

Applicants should demonstrate the following skills and knowledge:

• Ability to apply fundamental knowledge while following regulatory guidelines, global standard operating procedures (SOPs), and client expectations.

• Strong attention to detail and numerical accuracy.

• Analytical thinking, problem-solving skills, and sound judgment.

• Ability to work productively under direct supervision.

• Ability to maintain confidentiality of clinical data and clients’ proprietary information.

• Flexibility and adaptability when project requirements change.

• Ability to work independently and collaboratively within a team.

• Good written and verbal English communication skills.

• Computer proficiency, including Microsoft Word, Excel, and PowerPoint.

• Ability to extract relevant information from study documentation, protocols, and electronic clinical study data systems.

• Ability to identify trends in site and study data.

• Workload prioritization and planning skills to manage changing project demands.

• Understanding of project protocols, centralized monitoring plans, and other functional plans.

• Broad knowledge of clinical trial roles, functions, and processes.

• Understanding of medical and therapeutic areas and medical terminology.

Work Schedule & Environment

The position is listed with a second-shift afternoon schedule and an office work environment. The job page also categorizes the role as remote/hybrid, so candidates should review the official listing for the applicable work arrangement at their location.

The description mentions possible exposure to biological fluids and infectious organisms in clinical or laboratory environments, as well as electrical office equipment. Personal protective equipment, including protective eyewear, garments, and gloves, may be required depending on the working environment.

How to Apply

Interested candidates can review the complete job description and submit their applications through the official Thermo Fisher Scientific careers portal.

Apply here: Centralized Monitoring Analyst (Level I & II) – Official Job Posting

Review the official listing for the latest application status, location-specific requirements, and employment details.

Job Summary

Fortrea Recruitment 2026 – Supplier Qualification Senior Specialist

Fortrea is hiring a Supplier Qualification Senior Specialist for a 6-month contract position based in India. The opportunity is listed as remote, with Bangalore and Remote India shown as locations. Candidates with experience in clinical research, pharmaceutical quality assurance, document control, compliance, or regulated industry operations may be suitable for this role. Applications are open until 23 October 2026, with working hours from 2 PM to 11 PM IST.

Company Overview

Fortrea is a global contract research organization (CRO) that supports clinical development and research services. This role provides operational support for supplier qualification activities, documentation management, and compliance with established procedures.

Job Details

Job Role & Responsibilities

The selected candidate will support supplier qualification and re-qualification activities while maintaining accurate documentation and following standard operating procedures (SOPs).

Key responsibilities include:

• Support defined steps in supplier qualification and re-qualification processes.

• Collect, organize, and maintain supplier qualification documentation accurately.

• Enter and maintain supplier information in qualification tracking systems.

• Assist in preparing qualification packages for internal review.

• Support audit readiness by ensuring records are complete, current, and traceable.

• Escalate missing or inconsistent information according to established SOPs.

• Follow procedures supporting the end-to-end supplier qualification lifecycle.

Eligibility & Qualifications

Required educational qualifications: A bachelor’s degree in life sciences, healthcare, quality, or a related field, or equivalent experience.

Relevant courses may include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, B.Sc. Microbiology, M.Sc. Microbiology, or other relevant healthcare and life sciences qualifications. These are examples of potentially relevant courses, not a confirmed list of degrees accepted by Fortrea.

Experience Requirements

Applicants should have:

• 1–2 years of experience in a CRO, pharmaceutical company, clinical operations, quality assurance, or another regulated industry.

• Exposure to document control, compliance, or operational support.

• An understanding of basic Good Clinical Practice (GCP) principles.

• Professional, task-focused communication skills for working with internal stakeholders.

Fortrea may consider relevant and equivalent experience in place of the stated educational requirements.

Location, Work Mode & Timings

The position is listed as remote, with Bangalore and Remote India indicated as locations. Working arrangements are subject to the line manager’s requirements.

• Work mode: Remote-based, as requested by the line manager.

• Working hours: 2 PM to 11 PM IST.

• Contract duration: 6 months.

• Employment type: Full-time contract.

How to Apply

Interested and eligible candidates can apply through Fortrea’s official recruitment portal.

Application deadline: 23 October 2026

• Apply for Supplier Qualification Senior Specialist – Fortrea

• View the official job description

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

Job Summary

Reserve Bank of India Recruitment 2026 – Pharmacist on Contract, Mumbai

The Reserve Bank of India (RBI), Mumbai, invites applications to prepare a panel of 22 Pharmacists on a contract basis for dispensaries located across Mumbai and Navi Mumbai. Eligible candidates must hold a Diploma in Pharmacy (D.Pharm) or Bachelor of Pharmacy (B.Pharm) and be registered with the Maharashtra State Pharmacy Council. Applicants must also have at least two years of experience as a Pharmacist and basic computer knowledge. The engagement offers a fixed remuneration of ₹600 per hour, subject to a maximum of ₹3,000 per day, for a maximum period of 240 days.

Job Overview

About the Recruitment

RBI is preparing a panel of Pharmacists for its dispensaries in Mumbai and Navi Mumbai. This is a temporary contractual engagement, not a regular RBI employee position. Candidates placed on the panel may be engaged as and when the Bank requires their services, subject to medical fitness and acceptance of the applicable terms and conditions.

Category-Wise Vacancy Details

Eligibility & Qualifications

Candidates must satisfy the following requirements specified in the official advertisement.

Educational Qualifications

Applicants must have passed Matriculation or an equivalent examination and possess either of the following pharmacy qualifications:

• D.Pharm (Diploma in Pharmacy) from a recognized university, with registration under the Pharmacy Act, 1948.

• B.Pharm (Bachelor of Pharmacy).

Experience and Other Requirements

• Minimum 2 years of experience as a Pharmacist.

• Registration with the Maharashtra State Pharmacy Council.

• Basic working knowledge of computers.

• Experience with Public Sector Banks (PSBs), Public Sector Undertakings (PSUs), government organizations, or RBI will be given preference.

Salary and Remuneration

The engagement does not confer any right to a temporary or permanent position in RBI. The Bank may assign the Pharmacist to one or more dispensaries within its Mumbai and Navi Mumbai jurisdiction.

Selection Process

The recruitment process includes the following stages:

1. Shortlisting: Based on educational qualifications, residence distance from RBI dispensaries, and relevant work experience.

2. Interview: Shortlisted candidates will be called for an interview.

3. Medical examination: Candidates shortlisted after the interview will undergo a medical examination.

4. Document verification: Required certificates and supporting documents will be verified before engagement.

Being eligible does not guarantee an interview call or actual engagement from the panel.

How to Apply

Applicants must complete both application steps before the deadline.

Step 1: Submit the Online Details

Fill in the additional details through the online form provided by RBI.

Step 2: Send the Application by Post

Use the prescribed application format provided in Annex I of the official advertisement. Enclose photocopies of the required professional, academic, experience, age-proof, and other applicable certificates.

Postal address:

The Regional Director Human Resource Management Department, Recruitment Section Reserve Bank of India, Mumbai Regional Office Shahid Bhagat Singh Road, Fort Mumbai – 400001

The sealed envelope must be superscribed:

“Application for the post of Pharmacist on contract basis with fixed hourly remuneration, Mumbai”

• Last date: 3 November 2026

• Deadline time: 5:00 PM

• Applications must reach the stated address by the deadline.

Important Instructions

• Submit the application in the prescribed format.

• Include all required certificates and supporting documents.

• Ensure that the online details form is also completed.

• Candidates claiming SC, ST, OBC, or EWS reservation must submit the applicable certificates in the prescribed format.

• OBC candidates claiming reservation must satisfy the Non-Creamy Layer requirements and provide a certificate issued after 1 April 2026, as specified in the advertisement.

• No travel or other allowances will be paid for attending the interview.

For the complete advertisement and application instructions, visit the official RBI recruitment notice.

Job Summary

BIT Mesra Recruitment – Junior Research Fellow (JRF), Pharmaceutical Sciences

Birla Institute of Technology (BIT), Mesra, Ranchi, is inviting applications from eligible Indian nationals for one Junior Research Fellow (JRF) position in the Department of Pharmaceutical Sciences & Technology. The position is part of a Department of Health Research (DHR), Ministry of Health & Family Welfare, Government of India-funded research project focused on improving the palatability and oral bioavailability of antiepileptic drugs for pediatric patients. Candidates with a first-class M.Pharm, M.S., or M.Tech in the specified pharmaceutical disciplines and a valid GPAT, GATE, NET, or equivalent national-level examination qualification are eligible to apply. The fellowship is ₹37,000 per month, and applications must be submitted by 25 October 2026.

Job Overview

Research Project Details

Project Title: From Bitter to Better: Development of Polymer-Stabilized Nano-Cocrystal Suspensions of Antiepileptic Drugs for Improved Palatability and Oral Bioavailability in Pediatric Patients.

The project focuses on pharmaceutical formulation research aimed at improving the taste acceptability and oral bioavailability of antiepileptic medicines for pediatric patients.

Principal Investigator and Co-Principal Investigator

Principal Investigator (PI): Dr. Nimmy Kumari

• Designation: Assistant Professor

• Department: Pharmaceutical Sciences & Technology

• Institute: Birla Institute of Technology, Mesra, Ranchi, Jharkhand – 835215

• Email: nimmykumari@bitmesra.ac.in

Co-Principal Investigator: Dr. Sudeshna Kundu

• Designation: Assistant Professor

• Department: Pharmaceutical Sciences & Technology

• Institute: Birla Institute of Technology, Mesra, Ranchi, Jharkhand – 835215

• Email: sudeshnakundu@bitmesra.ac.in

Eligibility & Qualifications

Candidates must satisfy the essential qualifications specified in the official advertisement.

Required educational qualifications: First-class M.Pharm, M.S., or M.Tech in any of the following disciplines:

• M.Pharm in Pharmaceutics

• M.Pharm in Pharmaceutical Chemistry

• M.S. in the specified pharmaceutical disciplines

• M.Tech in Pharmaceutical Sciences & Engineering

• M.Tech in Pharmaceutical Technology (Formulations)

• Other qualifying M.Pharm, M.S., or M.Tech degrees in the disciplines explicitly listed in the advertisement

Mandatory examination qualification: Candidates must have a valid GPAT, GATE, NET, or equivalent national-level examination qualification.

Desirable qualification: Preference will be given to candidates with prior knowledge and research experience in Solid-State Pharmaceutics.

Fellowship and Project Duration

How to Apply

Eligible candidates must email their CV to the Principal Investigator and send a copy to the additional email address below.

Selection Process and Terms

• Candidates will be shortlisted based on their academic and professional background.

• Shortlisted candidates will receive an email with the date and time of the online interview.

• The selection committee’s decision will be final.

• The appointment will be governed by the applicable institute and funding-agency terms.

• No travel allowance or daily allowance (TA/DA) will be paid for attending the interview.

Job Summary

West-Coast Pharmaceutical Works Ltd. Recruitment – QC and QC-ADL Jobs, Gujarat

West-Coast Pharmaceutical Works Ltd. is inviting applications for positions in its Quality Control (QC) and QC-ADL departments at its Vadvaswami plant in Gujarat. Candidates with B.Sc. or M.Sc. qualifications and 0–2 years of experience can apply for these opportunities. The company specifies that candidates must have experience working with a pharmaceutical company. Interested applicants can submit their resumes to the HR email address or contact the recruitment team directly.

Job Overview

About the Company

West-Coast Pharmaceutical Works Ltd. is a pharmaceutical company promoting quality medicines and pharmaceutical manufacturing. The recruitment poster highlights opportunities to join its quality teams at the Vadvaswami plant in Gujarat.

Available Departments

1. Quality Control (QC)

The QC department opportunity is suitable for candidates with B.Sc. or M.Sc. qualifications and 0–2 years of experience, provided they have experience working in a pharmaceutical company.

2. QC-ADL Department

The QC-ADL department is also recruiting candidates with B.Sc. or M.Sc. qualifications and 0–2 years of pharmaceutical industry experience.

Eligibility & Qualifications

• Educational qualifications: B.Sc. or M.Sc.

• Relevant courses to consider: B.Sc. Chemistry, M.Sc. Chemistry, B.Sc. Analytical Chemistry, M.Sc. Analytical Chemistry, B.Sc. Biochemistry, M.Sc. Biochemistry, or other relevant scientific qualifications.

• Experience: 0–2 years.

• Industry requirement: Experience in a pharmaceutical company only.

The recruitment poster does not specify the exact eligible specializations, so the course examples above are suggested based on the QC and QC-ADL departments.

How to Apply

Interested candidates can send their updated resumes to the HR team or contact the recruitment representative.

Plant Address

West Coast Pharmaceuticals Works Limited Vadvaswami Plant, near Bhagwati Glass Factory, opposite Jogni Mata Temple, Denis Chem Lab, Vadvaswami Side Road, Chattral–Vadvaswami Road, Village Vadami, Taluka Kalol, District Gandhinagar, Gujarat – 382740.

Job Summary

Biomiicron Pharma India Recruitment – Product Executive, Chennai

Biomiicron Pharma India Pvt. Ltd. is inviting applications for the Product Executive position in its pharmaceutical marketing division in Chennai. The opportunity is open to B.Pharm and M.Pharm graduates, including freshers and experienced candidates. The role involves fieldwork, market research, product management, brand building, and new product launches. Candidates with good communication skills and a willingness to travel across India can apply by sending their resumes to the recruitment email addresses provided in the announcement.

Job Overview

Company Overview

Biomiicron Pharma India Pvt. Ltd. is an ISO 9001:2015-certified pharmaceutical company with WHO-GMP-approved manufacturing, as stated in the recruitment announcement. The company focuses on allopathic formulations and pharmaceutical marketing across India.

Job Role and Responsibilities

The Product Executive will support pharmaceutical product marketing, brand development, market research, and product launch activities.

Key responsibilities include:

• Fieldwork and market research: Conduct field visits and gather market insights.

• Product management: Support product lifecycle management and brand-related activities.

• Brand building: Contribute to brand promotion and marketing initiatives.

• Product development: Assist with product development activities.

• New product launches: Support planning and execution of product launch activities.

• Marketing campaigns: Participate in promotional campaigns and product marketing.

• Competitor analysis: Research market trends and competing products.

• Sales and regulatory coordination: Coordinate with sales and regulatory teams.

• Customer engagement: Support chemist interactions and customer engagement activities.

Eligibility & Qualifications

• Educational qualifications: B.Pharm or M.Pharm.

• Experience: Freshers and experienced candidates can apply.

• Gender: Open to male and female candidates.

• Communication: Good communication skills.

• Analytical skills: Ability to understand market information and support product-related decisions.

• Travel: Willingness to travel across India.

How to Apply

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

Job Summary

SCL Lifesciences Limited is inviting applications from eligible candidates to join its API pharmaceutical manufacturing team.
The company operates as a USFDA, WHO-GMP and EU-GMP approved active pharmaceutical ingredient (API) manufacturing facility.
This recruitment opportunity is based at Bhagwanpura, Derabassi, Punjab, for professionals interested in working in API manufacturing.
Interested candidates can submit their applications to the recruitment team using the email addresses or contact numbers provided below.

SCL Lifesciences Limited – Company Overview

SCL Lifesciences Limited is an API pharmaceutical manufacturing company with USFDA, WHO-GMP and EU-GMP approvals. The company is looking for talented professionals to support its growing manufacturing team at Bhagwanpura, Derabassi, Punjab.

SCL Lifesciences API Manufacturing Jobs

Department: Active Pharmaceutical Ingredients (API)

SCL Lifesciences Limited is inviting applications for opportunities in its API manufacturing team.

Eligibility & Qualifications

Candidates interested in API pharmaceutical manufacturing opportunities can contact the recruitment team to enquire about suitable positions and eligibility requirements.

Job Location

SCL Lifesciences Limited
Bhagwanpura, Derabassi, Punjab, India.

How to Apply

Interested candidates can send their updated CVs to the following email addresses:

• Email: avantika.chauhan@scllifesciences.com
• Email: hr@scllifesciences.com

Contact Numbers:

• 98759 94191
• 98759 94190

Candidates can contact the recruitment team for further information about available positions and application requirements.

Summary

Category	Details
Company	SCL Lifesciences Limited
Vacancies	API Manufacturing positions; specific designations not provided
Required Education	Not specified in the recruitment announcement
Experience	Not specified in the recruitment announcement

DAC55 Laboratories Pvt. Ltd. is inviting applications from eligible candidates for multiple positions across its pharmaceutical manufacturing facility.
The recruitment drive includes opportunities in Formulation Production, Quality Assurance (IPQA), Quality Control, Warehouse and Engineering departments.
Candidates with relevant experience in pharmaceutical production, quality operations, warehouse management and engineering can apply for suitable positions.
Interested applicants can share their CVs or contact the recruitment team using the details provided below.

DAC55 Laboratories Pvt. Ltd. – Company Overview

DAC55 Laboratories Pvt. Ltd. is recruiting professionals for various pharmaceutical manufacturing and support functions. The available positions cover formulation production, in-process quality assurance, quality control, warehouse operations and engineering services.

DAC55 Laboratories Production Jobs

Department: Formulation Production

Open Position: Officer

• Experience: 2–5 years
• Department Focus: Oral Solid Dosage (OSD) forms and external preparation

DAC55 Laboratories Quality Assurance Jobs

Department: Quality Assurance (IPQA)

Open Position: IPQA Officer

• Experience: 2–3 years
• Functional Area: In-Process Quality Assurance

DAC55 Laboratories Quality Control Jobs

Department: Quality Control

Open Position: Executive

• Experience: 3–5 years
• Functional Area: Pharmaceutical Quality Control

DAC55 Laboratories Warehouse Jobs

Department: Warehouse

Open Positions:

• Manager: 8–10 years of experience
• Officer: 2–3 years of experience

DAC55 Laboratories Engineering Jobs

Department: Engineering

Open Positions:

• ITI Electrician: 2–3 years of experience
• RO Operator: 2–3 years of experience
• ETP Operator: 2–3 years of experience

Eligibility & Qualifications

Candidates with relevant educational qualifications and practical experience in their respective departments can apply. The recruitment announcement specifies the required experience for each position but does not list individual educational qualifications.

How to Apply

Interested candidates can share their updated CV or contact DAC55 Laboratories using the following details:

• Email: hr@dac55india.com
• Contact Number: +91 8490041157

Applicants should mention their preferred department and position when contacting the recruitment team.

Summary

Category	Details
Company	DAC55 Laboratories Pvt. Ltd.
Vacancies	Formulation Production Officer, IPQA Officer, Quality Control Executive, Warehouse Manager, Warehouse Officer, ITI Electrician, RO Operator, ETP Operator
Required Education	Relevant qualifications for the respective pharmaceutical, warehouse and engineering roles
Experience	2–10 years, depending on the position