Maithri Drugs Private Limited is inviting applications for Quality Assurance (QA) positions, including Executive and Senior Executive.
Candidates with 1–7 years of experience in pharmaceutical quality assurance and related functions are eligible to apply.
The recruitment covers QA and AQA activities, including deviation management, change control, product quality reviews, validation, documentation and compliance.
Eligible candidates with relevant qualifications can attend the scheduled interviews at the company’s facility in Sangareddy, Telangana.

Maithri Drugs Private Limited – Company Overview

Maithri Drugs Private Limited is recruiting professionals for its Quality Assurance department. The company is seeking candidates with relevant experience in pharmaceutical quality systems, analytical data review, process validation and regulatory compliance.

Maithri Drugs Quality Assurance Jobs – Available Positions

Department: Quality Assurance (QA)

Available Positions:

• Executive
• Senior Executive

Job Description

Quality Assurance (QA)

• Deviation Management
• Change Control Management
• Annual Product Quality Review (APQR)
• Vendor Qualification
• Process and Cleaning Validation
• Marketing Complaint Handling
• Internal Audit Management
• In-Process Quality Assurance (IPQA)

Analytical Quality Assurance (AQA)

• Analytical Data Review
• Data Integrity Compliance
• Investigation Management
• Method Validation and Transfer
• Stability Program Oversight and Change Control Review
• Documentation Control
• Laboratory Compliance Monitoring
• Regulatory and Customer Support

Eligibility & Qualifications

Educational Qualifications

Eligible candidates should hold one of the following qualifications, depending on the position:

• B.Sc. (Chemical and Biotechnology)
• B.Pharm.
• B.Tech. (Chemical and Biotechnology)
• M.Sc.
• M.Pharm.

Experience

• 1–7 years of relevant experience.

Additional Eligibility

• Male candidates only.

Maithri Drugs Private Limited Interview Details

Interview Dates

• 17 October 2026 (Saturday)
• 24 October 2026 (Saturday)

Interview Timings

9:30 AM to 12:00 PM

Interview Venue

Maithri Drugs Private Limited,
Sy. No. 205, 222 to 226,
Bon thapally (V), Gummadidala (M),
Sangareddy (D), Telangana, India – 502313.

Contact Numbers

• 91-8455-694101
• 040-69076673

Benefits at Maithri Drugs Private Limited

• Free transportation
• Subsidized canteen
• Group personal accident policy
• Health insurance

How to Apply for Maithri Drugs Quality Assurance Jobs

Interested candidates can attend the interview on either of the scheduled dates. Applicants should carry their updated educational and employment documents, including:

• Educational certificates
• Employment-related documents
• Payslips for the latest three months
• Latest increment letter
• Appointment letter
• Previous relieving letters
• PAN card
• Aadhaar card

For further information, candidates can contact the recruitment team using the phone numbers listed above.

Summary

Category	Details
Company	Maithri Drugs Private Limited
Vacancies	Executive, Senior Executive
Required Education	B.Sc. (Chemical and Biotechnology), B.Pharm., B.Tech. (Chemical and Biotechnology), M.Sc., M.Pharm.
Experience	1–7 years

Eugia Pharma is conducting a walk-in interview for multiple positions at its Eugia Unit I facility in Shameerpet, Hyderabad.
The recruitment drive includes opportunities in Injectable Production, Oral Solid Dosage (OSD) Production, Quality Assurance and Quality Control.
Candidates with Diploma, B.Sc., B.Pharm., M.Pharm. and relevant postgraduate qualifications can apply for suitable positions based on their experience.
Eligible candidates with 3–12 years of experience are invited to attend the interview with their updated CV and supporting documents.

Eugia Pharma Recruitment – Company Overview

Eugia Pharma is inviting experienced pharmaceutical professionals to join its manufacturing and quality teams at Eugia Unit I, Shameerpet, Hyderabad. The recruitment drive covers production operations, injectable manufacturing, quality assurance and quality control activities.

Eugia Pharma Production Jobs – Injectable Manufacturing

Department: Production (Injectables)

Open Positions

• Production – Injectable (Filling, Compounding and Autoclave)

Candidates applying for injectable production roles should have relevant pharmaceutical manufacturing experience. The role covers activities related to filling, compounding and autoclave operations.

Eugia Pharma Production Jobs – Oral Solid Dosage (OSD)

Department: Production (OSD)

Open Positions

• Production – OSD

Candidates with relevant experience in pharmaceutical oral solid dosage manufacturing can apply for suitable positions in the OSD production department.

Eugia Pharma Quality Assurance Jobs

Department: Quality Assurance

Open Positions

• Quality Assurance (Injectable / Aseptic Area)

Candidates with relevant pharmaceutical quality assurance experience can apply for positions involving injectable manufacturing and aseptic area operations.

Eugia Pharma Quality Control Jobs

Department: Quality Control

Open Positions

• Quality Control (Stability, IP & FP)

Candidates with relevant quality control experience can apply for positions involving stability testing, in-process (IP) quality control and finished product (FP) quality control activities.

Eligibility & Qualifications

Candidates with the following qualifications can apply for relevant positions, depending on the specific role requirements:

Eligible Qualifications: Diploma | B.Sc. | B.Pharm. | M.Pharm. | Relevant postgraduate qualifications

Experience: 3–12 years, depending on the position.

Eugia Pharma Walk-In Interview Details

Interview Date and Time

• Date: Saturday, 17 October 2026
• Time: 9:30 AM to 2:30 PM

Interview Venue

Eugia Pharma Specialities Limited, Kolthur (V), Medchal (Dist.), Telangana – 500101.

Documents to Carry

Candidates should bring the following documents to the interview:

• Updated CV
• Educational certificates
• Recent payslips
• Latest increment letter
• CTC breakup
• Bank statement
• Aadhaar card

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue mentioned above. Carry an updated CV and the required supporting documents.

Candidates should check that their qualifications and experience match the requirements of their preferred department before attending the interview.

Summary

Category	Details
Company	Eugia Pharma Specialities Limited
Vacancies	Production – Injectable; Production – OSD; Quality Assurance – Injectable/Aseptic Area; Quality Control – Stability, IP & FP
Required Education	Diploma, B.Sc., B.Pharm., M.Pharm. and relevant postgraduate qualifications
Experience	3–12 years, depending on the position

Sunrise Remedies Pvt. Ltd. is inviting experienced candidates to attend a walk-in interview for multiple pharmaceutical positions.
The available openings include Production, Liquid Manufacturing, RM Store, Regulatory Affairs, Quality Assurance and Quality Control.
Candidates with qualifications such as B.Sc., M.Sc., B.Pharm., M.Pharm. and B.Com. can apply for relevant positions based on their experience and specialization.
Interested candidates should attend the walk-in interview with their updated CV and explore career opportunities with Sunrise Remedies.

Sunrise Remedies Pvt. Ltd. Recruitment – Company Overview

Sunrise Remedies Pvt. Ltd. is conducting a walk-in interview to recruit candidates across its pharmaceutical manufacturing, quality, regulatory and warehouse departments. The recruitment drive includes opportunities in capsule filling, liquid manufacturing, Ayurvedic production, analytical testing, in-process quality assurance and raw material store operations.

Sunrise Remedies Production Jobs – Capsule Filling

Department: Production

Position: Production (Capsule Filling)

Eligibility & Qualifications

• B.Sc.
• M.Sc.
• B.Pharm.
• M.Pharm.

Experience: 1–3 years

Salary: Up to ₹25,000 CTC per month

Sunrise Remedies Liquid Manufacturing Jobs

Department: Liquid Manufacturing

Position: Liquid Manufacturing

Eligibility & Qualifications

• M.Sc.
• B.Pharm.
• M.Pharm.

Experience: 2 years

Salary: Up to ₹25,000 CTC per month

Sunrise Remedies RM Store Jobs

Department: Raw Material (RM) Store

Position: Executive

Eligibility & Qualifications

• B.Com.
• M.Com.
• M.Sc.
• B.Pharm.
• M.Pharm.

Experience: 1–6 years

Salary: Up to ₹35,000 CTC per month

Sunrise Remedies Regulatory Affairs Jobs

Department: Regulatory Affairs

Position: Regulatory Affairs

Eligibility & Qualifications

• B.Pharm.
• M.Pharm.

Experience: 1–3 years

Salary: Up to ₹25,000 CTC per month

Sunrise Remedies QA Jobs – Ayurvedic Products

Department: Quality Assurance (QA)

Position: Senior Executive QA (Ayurvedic)

Eligibility & Qualifications

• B.Pharm. (Ayurvedic)
• M.Pharm. (Ayurvedic)

Experience: 3 years

Salary: Up to ₹35,000 CTC per month

Sunrise Remedies QC Jobs – HPLC

Department: Quality Control (QC)

Position: Senior QC Executive (HPLC)

Eligibility & Qualifications

• M.Sc.
• B.Pharm.
• M.Pharm.

Experience: 4–7 years

Salary: Up to ₹35,000 CTC per month

Sunrise Remedies Ayurvedic Production Jobs

Department: Production (Ayurvedic)

Position: Production

Eligibility & Qualifications

• B.Sc. Chemistry
• B.Sc. Botany
• B.Pharm. (Ayurvedic)

Experience: 2–3 years

Salary: Up to ₹25,000 CTC per month

Sunrise Remedies IPQA Jobs

Department: Quality Assurance (QA)

Position: QA Executive (IPQA)

Eligibility & Qualifications

• B.Pharm.
• M.Pharm.

Experience: 1–2 years

Salary: Up to ₹22,000 CTC per month

Sunrise Remedies QC Executive Jobs

Department: Quality Control (QC)

Position: QC Executive

Eligibility & Qualifications

• B.Sc.
• M.Sc.

Experience: 1–3 years

Salary: Up to ₹27,000 CTC per month

Eligibility & Qualifications

Candidates should hold the relevant qualification for their preferred position and have the required experience in pharmaceutical manufacturing, quality assurance, quality control, regulatory affairs or store operations.

Eligible qualifications: B.Sc. | M.Sc. | B.Pharm. | M.Pharm. | B.Com. | M.Com.

Sunrise Remedies Walk-In Interview Details

Interview Date and Time

• Date: Sunday, 18 October 2026
• Time: 10:00 AM to 4:00 PM

Interview Venue

Block No. 2244, Santej–Khatrāj Road, Opposite Shah Alloys Ltd., Santej, Gujarat – 382722.

Preferred Candidates

Candidates from Gujarat are preferred.

How to Apply

Interested and eligible candidates can attend the walk-in interview with their updated CV.

Contact Numbers:

• 96625 03881
• 76009 13422

Email: hr@sunriseremedies.in

Candidates should ensure their CV includes their educational qualifications, relevant experience, contact details and specialization matching the position.

Summary

Category	Details
Company	Sunrise Remedies Pvt. Ltd.
Vacancies	Production (Capsule Filling); Liquid Manufacturing; RM Store Executive; Regulatory Affairs; Senior Executive QA (Ayurvedic); Senior QC Executive (HPLC); Production (Ayurvedic); QA Executive (IPQA); QC Executive
Required Education	B.Sc., M.Sc., B.Pharm., M.Pharm., B.Com., M.Com.
Experience	1–7 years, depending on the position

 

AMNEAL Pharmaceuticals Recruitment – QA Apprentice, Ahmedabad

AMNEAL Pharmaceuticals is inviting applications from B.Pharm freshers for a Quality Assurance (QA) Apprentice position in its Oral Solid Dosage (OSD) Unit at SEZ Matoda, Pharmez, Ahmedabad, Gujarat. This apprenticeship is open to candidates who graduated in 2025 or 2026 and want to gain practical experience in pharmaceutical quality assurance. Selected candidates will receive a monthly stipend of ₹18,000, along with exposure to Good Manufacturing Practice (GMP), QA systems, and pharmaceutical manufacturing operations. Local candidates are preferred.

Job Overview

Key Responsibilities and Training

Selected apprentices can expect practical exposure to the following areas, based on the responsibilities described in the recruitment announcement:

• Quality Assurance systems in an Oral Solid Dosage (OSD) manufacturing unit.

• Good Manufacturing Practice (GMP) requirements.

• Pharmaceutical manufacturing operations.

• Documentation and quality-related procedures.

• Training and guidance from experienced QA professionals.

Facilities and Benefits

• Monthly stipend: ₹18,000.

• Transportation: Facility provided.

• Canteen: Facility provided.

• Training: Practical exposure to pharmaceutical QA and GMP.

• Career development: Potential future employment based on performance and organizational requirements.

How to Apply

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

Applicants should include their B.Pharm qualification, passing year (2025 or 2026), and contact details in their resume.

Job Summary

FDC Limited Recruitment – Analytical R&D Jobs, Mumbai

FDC Limited is inviting applications for multiple positions in its Analytical Research and Development (ARDL) Department at Andheri (West), Mumbai. The available designations are Officer, Senior Officer, and Executive. Candidates with an M.Sc. or M.Pharm in Analytical Chemistry and relevant experience in analytical research and development may be suitable for these opportunities. Interested applicants can submit their details through the online application form provided by the company.

Job Overview

Company Overview

FDC Limited is a pharmaceutical company. Through its Analytical R&D department, the company is seeking professionals who can contribute to analytical research and scientific quality standards.

Available Positions

1. Officer – Analytical R&D

Suitable for candidates with a relevant analytical chemistry qualification and experience aligned with the department’s requirements.

2. Senior Officer – Analytical R&D

An opportunity for experienced professionals seeking to contribute to analytical research and development activities.

3. Executive – Analytical R&D

A position for candidates with relevant qualifications and experience in analytical research.

Eligibility & Qualifications

Candidates should have one of the following qualifications:

M.Sc. Analytical Chemistry or M.Pharm in Analytical Chemistry.

Applicants should have relevant experience and an interest in analytical research and scientific excellence.

How to Apply

Interested candidates can submit their applications through the online form shared in the recruitment announcement.

Job Summary

IKS Health Recruitment – Medical Scribe (Clinical Documentation Specialist)

IKS Health is hiring Medical Scribes (Clinical Documentation Specialists) for multiple locations across India, including Mumbai, Hyderabad, Chennai, Coimbatore, and Visakhapatnam. This opportunity is suitable for candidates with at least one year of Live Scribe experience who are interested in clinical documentation and healthcare support services. The position requires working night shifts from the office, with pick-up and drop facilities provided. Interested candidates can contact HR representative Pooja Patil directly using the contact details in the recruitment announcement.

Job Overview

Role and Responsibilities

A Medical Scribe, also known as a Clinical Documentation Specialist, supports clinical documentation workflows. The recruitment announcement does not provide a detailed list of daily responsibilities, so candidates should confirm the specific duties with the hiring team.

Eligibility & Qualifications

• Experience: Minimum one year of Live Scribe experience.

• Relevant background: Candidates with experience in live medical scribing and clinical documentation may consider this opportunity.

• Work schedule: Willingness to work night shifts from the office.

The supplied announcement does not specify mandatory educational qualifications. Candidates should confirm the required qualification directly with HR before applying.

How to Apply

Interested candidates can contact Pooja Patil, HR, using the details below.

Applicants should share their updated CV and mention their Live Scribe experience and preferred job location.

Job Summary

Catalyst Clinical Services Recruitment – Clinical Research Coordinator (CRC), New Delhi

Catalyst Clinical Services is hiring one Clinical Research Coordinator (CRC) for its site in New Delhi. This opportunity is suitable for candidates with a Pharmacy or Life Sciences qualification and clinical research coordination experience. Applicants should have at least one year of experience as a CRC, along with knowledge of ICH-GCP, NDCT Rules, bioethics, and end-to-end clinical trial processes. Candidates who have completed the Professional Diploma in Clinical Research (PDCR) are eligible for an experience waiver, according to the recruitment announcement.

Job Overview

Company Overview

Catalyst Clinical Services operates in the clinical research sector. For this opening, the company is seeking a Clinical Research Coordinator to support clinical research activities at its New Delhi site.

Eligibility & Qualifications

Candidates should meet the following requirements mentioned in the recruitment announcement:

• Educational qualifications: Bachelor’s or master’s qualification in Pharmacy or Life Sciences.

• Relevant courses to consider: 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 related qualifications.

• Experience: Minimum one year of experience working as a Clinical Research Coordinator (CRC).

• Experience waiver: Candidates who have completed the Professional Diploma in Clinical Research (PDCR) are eligible for a waiver of the experience requirement, as stated in the advertisement.

• Clinical research knowledge: Strong knowledge of ICH-GCP, New Drugs and Clinical Trials (NDCT) Rules, bioethics, and end-to-end clinical trial processes.

How to Apply

Interested candidates can email their updated CV to the recruitment team.

Applicants should include their relevant clinical research experience and qualifications in their CV.

Job Summary

Merck Recruitment – Senior Associate, Clinical Research

Merck is inviting applications for the Senior Associate, Clinical Research position within its clinical research operations. This role focuses on clinical trial administration, site start-up, essential document management, regulatory submissions, clinical trial budgets, contracts, and investigator payments. Candidates with relevant clinical research experience, knowledge of ICH-GCP guidelines, and strong documentation, communication, and organizational skills may find this opportunity suitable. The job posting lists 22 October 2026 as the closing date, so applicants should check the official careers page and apply before the deadline.

Job Overview

Location note: The supplied posting does not identify a specific work location for this vacancy. It is listed on MSD’s international careers website for Europe, the Middle East, Africa, Latin America, and Asia Pacific.

Company Overview

Merck Sharp & Dohme (MSD), also known as Merck & Co., Inc. in the United States and Canada, is a global healthcare company involved in pharmaceutical research and development. Its clinical research teams support the operational activities required to conduct clinical trials in accordance with applicable regulatory requirements and research guidelines.

The Senior Associate, Clinical Research role supports study administration, documentation, regulatory and site start-up activities, financial coordination, and communication with investigators and other clinical research stakeholders.

Job Role and Responsibilities

The Senior Associate will support clinical trial operations by coordinating study documentation, site activities, regulatory submissions, budgets, contracts, and meetings.

1. Trial and Site Administration

• Track essential clinical trial documents and report safety reports.

• Coordinate the collection and distribution of study tools and documents.

• Update Clinical Trial Management Systems (CTMS) and study trackers.

• Coordinate clinical and non-clinical supply management with other country-level team members.

• Manage labeling requirements and coordinate translation change requests, where applicable.

2. Clinical Trial Document Management

• Prepare clinical trial documents and correspondence.

• Distribute, ship, and archive clinical documents, including electronic Trial Master File (eTMF) records.

• Assist with eTMF reconciliation and execute the eTMF Quality Control Plan.

• Update study manuals, patient diaries, instructions, and related documents.

• Maintain documentation confirming the proper destruction of clinical supplies.

• Prepare investigator trial file binders.

• Coordinate document translations.

3. Regulatory Affairs and Site Start-Up

• Collect and provide forms and lists required for site evaluation, validation, site start-up, and regulatory submissions.

• Obtain, track, and update study insurance certificates.

• Support preparation of submission packages for Institutional Review Boards (IRBs) and Ethics Review Committees (ERCs).

• Assist with submissions to regulatory agencies.

• Publish study results for GCTO and Regulatory Affairs (RA) where required by local legislation.

4. Budgeting, Contracts and Payments

• Develop, monitor, update, and close country and site budgets, including split-site budgets.

• Develop, negotiate, approve, and maintain Clinical Trial Research Agreements (CTRAs).

• Track and report contract negotiations.

• Maintain contract templates in collaboration with the Legal Department.

• Calculate and process payments to investigators, vendors, and grant recipients.

• Follow financial and compliance procedures.

• Monitor compliance and disclosure requirements.

• Maintain financial tracking tools.

• Obtain and process Foreign Corrupt Practices Act (FCPA) documentation within required timelines.

5. Meeting Planning

• Organize meetings and prepare or track study memos, letters, and protocols.

• Support local investigator meetings.

Eligibility & Qualifications

The supplied job description does not specify a mandatory academic qualification or a minimum number of years of experience. Candidates should review the official vacancy requirements before applying.

Relevant courses to consider: B.Pharm, M.Pharm, Pharm.D, B.Sc. Clinical Research, M.Sc. Clinical Research, 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 potentially relevant academic backgrounds for clinical research work, not a confirmed list of qualifications accepted by MSD for this vacancy.

Key Skills Required

• Knowledge of clinical research guidelines and ICH-GCP.

• Good Documentation Practices (GDP) and clinical trial document management.

• Strong Microsoft Office skills, particularly Microsoft Excel.

• Familiarity with Clinical Trial Management Systems (CTMS) and other clinical IT applications.

• Understanding of clinical trial operations, compliance, and regulatory submissions.

• Budget development, contract processing, and payment coordination skills.

• Excellent written and verbal communication in business English and relevant local languages.

• Strong negotiation, time management, and organizational skills.

• Ability to manage competing priorities and work independently.

• Problem-solving, conflict management, and decision-making abilities.

• Ability to collaborate effectively with investigators, study sites, finance teams, and multicultural stakeholders.

• Accountability, customer focus, adaptability, and a proactive approach to resolving issues.

Employment Details and Application Deadline

The vacancy is listed as a regular employment position. The supplied posting does not provide confirmed details for salary, visa sponsorship, relocation, shift timings, or travel requirements.

Application deadline: 22 October 2026.

According to the job posting, applications must be submitted no later than the day before the listed end date, so candidates should aim to apply by 21 October 2026.

 

How to Apply

Interested candidates can review the complete vacancy details and check their eligibility through the official MSD careers portal.

Apply Online – Senior Associate, Clinical Research at MSD

Current employees and contingent workers should use the dedicated internal application links provided in the original posting.

Job Summary

Colgate-Palmolive Recruitment – Associate Scientist, Toxicology, Mumbai

Colgate-Palmolive is inviting applications for the Associate Scientist, Toxicology position in Mumbai, Maharashtra. This on-site opportunity is suitable for candidates with a postgraduate qualification in Toxicology, Pharmacology, or a related scientific discipline. Applicants must have at least one year of industry experience in toxicology, preferably in consumer products, pharmaceuticals, medical devices, or the food industry. The role involves product safety reviews, toxicological literature searches, scientific database evaluation, and safety assessments to support product compliance.

Job Overview

Company Overview

Colgate-Palmolive is a global consumer products company operating in more than 200 countries. Its business includes Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition.

The company focuses on innovation, consumer safety, and developing products that support healthier futures for people and their pets. In this role, the selected candidate will join the Global Product Safety team and provide toxicology support to colleagues based in Piscataway, United States.

Job Role and Responsibilities

The Associate Scientist, Toxicology will support product safety assessments and help ensure that formulas and human-use studies meet applicable safety requirements.

Product Safety Reviews

• Review new product formulas and experimental recipes for safety clearance.

• Evaluate formulas intended for clinical, consumer, and panel studies involving human use protocols.

• Support product safety assessments to help protect consumers and ensure compliance.

Toxicological Assessments and Reporting

• Prepare Product Safety Reports.

• Assist senior toxicologists with formula reviews and comparisons.

• Support the preparation of product registration safety letters and responses to regulatory requests.

Scientific Literature and Database Evaluation

• Search toxicological and scientific databases to support raw material safety assessments.

• Evaluate relevant scientific literature and available data.

• Assist with safety evaluations of new raw materials.

Product Data Management

• Maintain Compliance Check values in Colgate’s Product Data Management (PDM) system.

• Coordinate with the Global Product Safety team to support consistent product safety review activities.

Shift Requirements

The position requires working hours that overlap with the US-based Global Product Safety team in Piscataway. Candidates should be prepared to work according to the assigned shift schedule.

Eligibility & Qualifications

Educational Qualifications

Candidates must hold a master’s-level qualification in Toxicology, Pharmacology, or a related scientific discipline.

Relevant courses to consider: M.Sc. Toxicology, M.Sc. Pharmacology, M.Pharm Pharmacology, M.Sc. Pharmaceutical Sciences, M.Sc. Biochemistry, M.Sc. Biotechnology, M.Sc. Life Sciences, or another closely related scientific postgraduate qualification.

The employer specifically names Toxicology, Pharmacology, or a related discipline. The additional course examples are potential matches, not an official list of accepted qualifications.

Experience Requirements

• Minimum 1 year of industry experience in Toxicology, preferably involving consumer products.

• Experience in Product Safety or Toxicology within a consumer products, medical device, food, or pharmaceutical company.

Required Skills

• Strong written and verbal communication skills in English.

• Relationship-building and effective execution skills.

• Ability to conduct scientific literature searches.

• Experience evaluating toxicological and scientific databases.

• Understanding of product safety assessment and toxicological data.

What Colgate-Palmolive Offers

• Relocation assistance within India.

• Opportunity to work with the Global Product Safety team.

• Exposure to product safety assessments and toxicology activities in a global consumer products company.

• Collaboration with toxicologists and other scientific professionals.

How to Apply

Interested candidates can review the full job description and submit their applications through the official Colgate-Palmolive careers portal.

Apply Online – Associate Scientist, Toxicology

Job Summary

Grifols Recruitment – Regulatory and Quality Specialist, Gurgaon

Grifols is inviting applications for the Regulatory and Quality Specialist position in Gurgaon, India. This full-time opportunity is suited to professionals with experience in pharmaceutical regulatory affairs, regulatory submissions, and quality assurance. The role also involves supporting local pharmacovigilance activities and ensuring compliance with Indian and regional regulatory requirements. Candidates with a Pharmacy or Life Sciences qualification, knowledge of regulatory authorities, and strong communication skills may find this opportunity relevant.

Job Overview

Company Overview

Grifols is a global healthcare company established in 1909. It specializes in plasma-derived medicines and transfusion medicine, developing, manufacturing, and marketing healthcare products and services in more than 110 countries and regions.

The company offers professionals an opportunity to collaborate with local, regional, and global teams while contributing to regulatory compliance and healthcare operations.

Job Role and Responsibilities

The Regulatory and Quality Specialist will lead Regulatory Affairs activities for India and neighbouring markets while supporting local Quality Assurance and Pharmacovigilance functions. The role focuses on product registration, regulatory compliance, quality systems, and lifecycle management.

Regulatory Affairs

• Manage product registrations, regulatory submissions, approvals, renewals, and lifecycle activities.

• Monitor regulatory developments and maintain regulatory intelligence.

• Liaise with health authorities in India and neighbouring markets.

• Develop and implement regulatory strategies aligned with business objectives.

• Support product launches, portfolio maintenance, pricing activities, and tender participation.

Quality Assurance

• Support compliance with local Quality Management System (QMS) requirements.

• Assist with audits and supplier qualification activities.

• Support Good Distribution Practice (GDP) activities.

• Oversee quality-related requirements for third-party logistics providers.

Pharmacovigilance

• Act as a local backup contact for Pharmacovigilance activities.

• Support compliance with local and global pharmacovigilance requirements.

• Assist with safety reporting and maintenance of pharmacovigilance procedures.

Cross-Functional Collaboration

• Work closely with Commercial, Medical Affairs, Supply Chain, Finance, and global teams.

• Support business growth while maintaining regulatory and quality compliance.

• Coordinate with relevant stakeholders in a multicultural working environment.

Eligibility & Qualifications

Applicants should meet the following requirements:

• Educational qualifications: 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, B.Sc. Biochemistry, M.Sc. Biochemistry, or another related scientific qualification.

• Regulatory Affairs experience: Professional experience in the pharmaceutical, biotechnology, medical device, or healthcare industry.

• Regulatory knowledge: Understanding of regulatory submissions, product approvals, and interactions with health authorities, preferably in India and SAARC countries.

• Communication: Strong stakeholder management, communication, and organizational skills.

• Language proficiency: Fluency in Hindi and English.

• Technical skills: Experience with Veeva, SAP, TrackWise, or similar regulatory and quality management systems is an advantage.

The employer specifies a degree in Pharmacy, Life Sciences, or a related scientific discipline. The individual courses listed above are examples of potentially relevant qualifications, not a confirmed employer-approved course list.

What Grifols Offers

• Competitive benefits package.

• Permanent employment contract.

• Collaboration with local, regional, and global teams.

• Professional development opportunities within a multinational healthcare organization.

• Exposure to Regulatory Affairs, Quality Assurance, and Pharmacovigilance functions.

How to Apply

Interested candidates can review the requirements and submit their application through the official Grifols careers portal.

Apply Online – Grifols Regulatory and Quality Specialist

Job Summary