Category: Featured

Amgen Hiring – Data Management Sr Associate | Clinical Development | Hyderabad

Amgen is hiring a Data Management Sr Associate for its Clinical Development team in Hyderabad. The role focuses on supporting high-quality clinical trial data delivery through database build testing, data cleaning, query management, reconciliation, and lock preparation across the clinical study lifecycle.

Company Overview

Amgen is a biotechnology company focused on developing medicines for serious illnesses across areas including Oncology, Inflammation, General Medicine, and Rare Disease. The company describes its culture as collaborative, innovative and science-based.

Data Management Sr Associate – Clinical Development

Job Details

• Position: Data Management Sr Associate
• Career Category: Clinical Development
• Location: Hyderabad, India
• Work Mode: On Site
• Employment Type: Full Time
• Job Requisition ID: R-255251

Job Responsibilities

Clinical Data Management

• Execute study data management activities across the clinical study lifecycle.
• Perform database build testing, data cleaning, query management, reconciliation and lock preparation with limited oversight.
• Support core Data Management roles, including:

  • Data Delivery Leads
  • Database Designers
  • Data Acquisition Leads

• Own time-sensitive deliverables and ensure high-quality execution.
• Contribute to the setup and maintenance of EDC/non-CRF data structures.
• Support local laboratories, coding dictionaries and non-CRF data integrations.

Study Timelines & Data Delivery

• Track progress against data management timelines, study timelines and deliverables.
• Identify potential risks or delays.
• Escalate issues with clear documentation and applicable mitigations.
• Coordinate with local internal teams, global team members and external partners, including FSPs, when required.
• Help ensure aligned and efficient delivery of study activities.

Process Improvement

• Identify opportunities to improve repeatable data management processes.
• Contribute to best practices and knowledge sharing across the team.

Eligibility & Qualifications

Basic Qualifications

Candidates must meet one of the following requirements:

• Master’s degree, or
• Bachelor’s degree with 2 years of clinical execution experience, or
• Associate’s degree with 6 years of clinical execution experience, or
• High school diploma/GED with 8 years of clinical execution experience

Preferred Qualifications

• 3 years of work experience in a life sciences or medically related field.
• At least 1 year of biopharmaceutical clinical research experience obtained through clinical trials in a biotechnology, pharmaceutical or CRO company.
• Experience working in Data Management on global clinical trials.

Eligible Qualification Courses

Master’s Degree | Bachelor’s Degree | Associate’s Degree | Relevant Life Sciences Qualifications

The source specifies degree levels rather than particular courses such as B.Pharm, M.Pharm or Pharm.D, so specific pharmacy courses have not been added as a mandatory requirement.

Location & Work Mode

Location: Hyderabad, India
Work Mode: On Site
Employment: Full Time

The supplied job posting identifies the role as On Site.

How to Apply

Interested and eligible candidates can apply through the official Amgen careers portal.

Apply for Data Management Sr Associate – Amgen

Job Summary

GlobalData Hiring – Analyst / Senior Analyst | Healthcare | Hyderabad

GlobalData is hiring Analysts and Senior Analysts for its Healthcare – Pharma team in Hyderabad. The role focuses on researching advanced drug modalities such as ADCs, cell and gene therapies, bispecific antibodies, and RNA-based therapies, and capturing detailed scientific information for pharmaceutical and biotech intelligence databases.

Company Overview

GlobalData is a productivity and intelligence platform that combines proprietary data, human expertise, and AI to support organizations with strategic planning, innovation, risk management, and sustainable growth.

The Healthcare – Pharma team is expanding its coverage of advanced drug modalities and is looking for researchers with strong scientific knowledge and a structured, detail-oriented approach.

Analyst / Senior Analyst – Healthcare

Position Details

• Position: Analyst / Senior Analyst
• Team: Healthcare – Pharma
• Location: Hyderabad
• Work Area: Drug intelligence, scientific research, data curation and taxonomy

Education

Candidates should have one of the following qualifications:

• M.Pharm or M.S. (Pharm) in Pharmacology, Biotechnology or a related specialisation
• M.Sc. or M.Tech in Biotechnology, Biochemistry, Molecular Biology, Immunology, Genetics, Microbiology or a related life-science discipline
• PhD in a relevant field such as Immunology, Cell and Gene Therapy, Nucleic Acid Chemistry or Antibody Engineering

Experience

• 2–5 years of relevant experience in:

  • Pharmaceutical or biotech R&D
  • Academic research
  • CROs
  • Pharmaceutical intelligence
  • Scientific data curation

• Candidates with a PhD and 2+ years of industry or postdoctoral experience are also encouraged to apply.
• Hands-on laboratory or research experience in at least one advanced modality is strongly preferred.
• Relevant modalities include:

  • Cell therapy
  • Gene therapy or gene editing
  • Antibody-drug conjugates (ADCs)
  • Nucleic acid therapies
  • Antibody engineering

• Experience in cell-based therapies is particularly valued.
• Experience with taxonomy or ontology development, biomedical data curation or scientific classification is highly desirable.

Scientific Knowledge & Skills

Candidates should have:

• In-depth understanding of at least one advanced drug modality and working knowledge of others.
• Strong foundation in molecular biology, immunology and pharmacology.
• Understanding of drug targets and mechanisms of action.
• Good knowledge of the drug development lifecycle, from discovery through post-marketing.
• Familiarity with drug naming conventions, including WHO INN nomenclature for biologics and cell and gene therapies.

Taxonomy & Data Skills

• Ability to break complex scientific information into well-defined and mutually exclusive attributes.
• Understanding of taxonomy principles, including:

  • Hierarchies
  • Controlled vocabularies
  • Synonym management

• Familiarity with MeSH, NCI Thesaurus, Gene Ontology or ChEBI is an advantage.
• Advanced Microsoft Excel skills, including pivot tables, lookups and data validation.
• Basic SQL or scripting knowledge is an advantage.
• Ability to use AI-assisted research tools responsibly and verify their output carefully.

Research & Communication

• Strong systematic secondary research skills across:

  • PubMed
  • Clinical trial registries
  • Patent databases
  • Regulatory sources
  • Conference abstracts and presentations

• Strong attention to detail and critical-thinking skills.
• Ability to identify incorrect, incomplete or conflicting information.
• Clear written English and ability to document definitions, rules and decision rationale.
• Ability to work independently as well as within a global team.
• Ability to manage multiple assignments and meet deadlines.

Key Responsibilities

Modality Research & Data Capture

• Conduct in-depth secondary research on drugs across different modalities and development stages.
• Research drug development from discovery and preclinical stages through clinical development and approval.
• Extract detailed technical attributes such as:

  • Construct design
  • Delivery systems
  • Chemistry
  • Engineering features

• Research information from scientific publications, conference abstracts and posters, patents, clinical trial registries, regulatory documents and company disclosures.
• Interpret complex, incomplete or ambiguous technical information and determine what can be reliably captured.
• Maintain clear source references.
• Track new drugs, pipeline events and emerging technologies within assigned modalities.

Taxonomy Development & Classification

• Contribute to the design and development of modality taxonomies.
• Develop hierarchical categories, attribute fields, controlled vocabularies and permitted values.
• Write definitions, inclusion and exclusion criteria, and classification rules.
• Build and maintain synonyms and naming conventions.
• Classify and map drugs to the relevant taxonomy.
• Apply classification rules consistently across records.
• Document curation guidelines, decision logs and worked examples.

Data Quality & Database Management

• Create, review and update drug records in GlobalData databases.
• Identify missing, outdated or inconsistent information.
• Cross-check information across multiple sources.
• Perform quality checks on research and database outputs.
• Flag data-quality issues and work with relevant team members to resolve them.

Collaboration & Delivery

• Work with analysts, subject matter experts and managers to resolve scientific and classification questions.
• Collaborate with product, data and technology teams to translate taxonomies into database structures and search features.
• Share modality knowledge with the wider team.
• Support quality improvement initiatives.
• Manage assigned work and deliver within agreed timelines.
• Collaborate with global teams across different time zones.

Eligible Qualification Courses

M.Pharm | M.S. (Pharm) | M.Sc. Biotechnology | M.Sc. Biochemistry | M.Sc. Molecular Biology | M.Sc. Immunology | M.Sc. Genetics | M.Sc. Microbiology | M.Tech Biotechnology | PhD in relevant field

How to Apply

Interested and eligible candidates can apply through the official GlobalData careers listing for Analyst / Senior Analyst – Healthcare in Hyderabad.

Apply for Analyst / Senior Analyst – Healthcare at GlobalData

Job Summary

Fresenius Kabi Hiring – Aggregate Medical Writer | Pharmacovigilance

Fresenius Kabi is hiring Aggregate Medical Writers for its Global Vigilance team in Gurgaon. The opportunity is suitable for professionals with 1–4 years of pharmacovigilance experience and expertise in authoring aggregate safety reports. Candidates with experience in PSURs, PBRERs, ACOs, PADERs, RMPs, and Signal Reports can apply.

Company Overview

Fresenius Kabi is hiring experienced professionals for its Global Vigilance – Gurgaon team. The position involves authoring and reviewing aggregate safety reports and conducting literature reviews to identify signals and significant safety information.

Aggregate Medical Writer – Global Vigilance

Job Responsibilities

• Perform authoring and review of safety reports, including:

  • PSURs
  • PBRERs
  • RMPs
  • ACOs
  • PADERs

• Perform literature reviews to identify signals and significant safety information.

Eligibility & Qualifications

• PhD
• BDS
• M.Pharm
• Pharm.D
• Only the above qualifications are eligible, as specified in the recruitment details.

Experience

• 1–4 years of experience in Pharmacovigilance
• Expertise in authoring aggregate reports
• Experience with PSURs/PBRERs, ACOs, PADERs, RMPs, and Signal Reports

Behavioral Competencies

• Excellent interpersonal communication and writing skills
• Experience handling cross-functional projects
• Ability to work effectively in a multi-cultural and global work environment

Location & Work Mode

Location: Gurgaon
Department: Global Vigilance
Work Mode: Work from office is mandatory, with a one-day flexi working option.

How to Apply

Interested and eligible candidates can share their updated resume with:

Email: Sonia.Kaushik@ext.fresenius-kabi.com

Job Summary

Genotypic is hiring an Executive – Genomics Services Sales for its South and East India business operations.
The role is suitable for Life Science postgraduate freshers and candidates with up to 2 years of experience.
The position focuses on client engagement, business development, solution selling, and promoting genomics services to academic and government research organizations.
Candidates with an M.Sc. in Life Sciences, Biotechnology, Molecular Biology, Genomics, or related fields can apply for this opportunity in Bengaluru.

Genotypic Genomics Services Sales: Executive

Position Details

• Department: Genomics Services Sales
• Position: Executive
• Region: South and East India
• Location: Bengaluru
• Experience: 0–2 Years
• Industry: Genomics / Life Sciences

Genotypic Genomics Services Sales: About the Role

The role is designed for Life Science postgraduates who have an interest in both science and business development. The selected candidate will work with researchers and academic institutions, understand their genomics requirements, and promote relevant genomics services and solutions.

The position involves building client relationships, identifying business opportunities, participating in industry events, and supporting sales activities across the assigned region.

Genotypic Genomics Services Sales: Key Responsibilities

Identify & Engage

• Prospect and qualify leads from academic institutions.
• Identify potential opportunities among researchers and research organizations.

Client Interaction

• Engage with researchers and understand their genomics and research requirements.
• Communicate relevant genomics services based on client needs.

Relationship Building

• Develop strong relationships with scientists, researchers, and key decision-makers.
• Maintain professional relationships with existing and prospective clients.

Solution Selling

• Present and promote relevant Genomics Services & Solutions.
• Understand client requirements and communicate suitable service offerings.

Sales Execution

• Drive sales activities and work towards achieving assigned targets.
• Support business development activities across the assigned territory.

Industry Participation

• Attend conferences and seminars.
• Participate in client meetings and relevant industry interactions.

Genotypic Genomics Services Sales: Skills Required

Communication & Interpersonal Skills

• Strong communication and interpersonal skills.
• Ability to interact professionally with researchers and decision-makers.

Business Development

• Passion for client-facing roles and business development.
• Target-driven and proactive mindset.
• Ability to build and maintain professional relationships.

Scientific Knowledge

• Basic understanding of genomics and life science services.
• Strategic thinking and problem-solving ability.

Genotypic Genomics Services Sales: Eligibility & Qualifications

Educational Qualification

M.Sc Life Sciences | M.Sc Biotechnology | M.Sc Molecular Biology | M.Sc Genomics

Candidates with an M.Sc. in Life Sciences, Biotechnology, Molecular Biology, Genomics, or related fields are eligible to apply.

Experience

0–2 Years

Freshers with the required postgraduate qualification can apply. Candidates with up to 2 years of relevant experience may also be considered.

Job Requirements

• M.Sc. in Life Sciences, Biotechnology, Molecular Biology, Genomics, or related fields.
• Strong interest in sales and business development.
• Eagerness to learn, grow, and build a career at the intersection of science and business.
• Strong communication and interpersonal skills.
• Basic understanding of genomics and life science services.

Genotypic Genomics Services Sales: Career Opportunity

This position offers an opportunity for Life Science postgraduates to work at the intersection of genomics, scientific services, client engagement, and business development.

The selected candidate will interact with academic institutions, researchers, scientists, and other stakeholders while developing knowledge of genomics services and commercial applications.

How to Apply

Interested candidates can apply by sending their updated resume to:

Email: jobs@genotypic.co.in

Application Subject

Position Applied – Surname

Candidates should mention the position applied for clearly in the email subject and provide their relevant educational and professional details in the resume.

Job Summary

Zydus Lifesciences Limited is conducting a walk-in interview at Indore for experienced professionals for its SEZ-II Unit, Ahmedabad.
The recruitment covers opportunities across Production, Engineering, Packing, Warehouse, Quality Control and Quality Assurance departments.
Candidates with ITI, Diploma, B.Sc, B.Pharm, B.E. and B.Tech qualifications and 3–8 years of experience can apply for the relevant positions.
The walk-in interview is scheduled for 4 October 2026, from 9:00 AM to 3:00 PM, at Papiya Tree Hotel, Indore, Madhya Pradesh.

Zydus Lifesciences Production Department: Plant Operator / Technical Assistant

Position Details

• Department: Production
• Position: Plant Operator / Technical Assistant
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

Candidates are required for production operations involving:

• Granulation – ACE, GEA
• Compression – Fette Kilian
• Wurster – Glatt
• Continuous Coater – DHARA

Eligibility & Qualifications

ITI | Diploma | B.Sc | B.Pharm

Candidates with relevant experience in pharmaceutical production operations can apply.

Zydus Lifesciences Engineering Department: Executive / Senior Executive

Position Details

• Department: Engineering
• Position: Executive / Senior Executive
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• Process Equipment – Mechanical & Electrical
• Utility – Air Compressor, Chiller & Boiler

Eligibility & Qualifications

Diploma | B.E. | B.Tech | ITI

Candidates with relevant experience in pharmaceutical engineering, process equipment or utility operations can apply.

Zydus Lifesciences Engineering Department: Operator / Technician

Position Details

• Department: Engineering
• Position: Operator / Technician
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• BMS / HVAC
• Process Equipment – Fitter & Electrician
• Utility & Water System

Eligibility & Qualifications

ITI | Diploma | B.E. | B.Tech

Candidates with relevant experience in BMS, HVAC, process equipment, electrical, fitting, utility or water systems can apply.

Zydus Lifesciences Packing Department: Plant Operator / Technical Assistant

Position Details

• Department: Packing
• Position: Plant Operator / Technical Assistant
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Area

CVC Bottle Line

Eligibility & Qualifications

ITI | Diploma | B.Sc

Candidates with relevant experience in pharmaceutical packing operations and CVC bottle lines can apply.

Zydus Lifesciences Packing Department: Officer / Senior Executive

Position Details

• Department: Packing
• Position: Officer / Senior Executive
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Area

CVC Bottle Line

Eligibility & Qualifications

Diploma | B.Sc | B.Pharm

Candidates with relevant experience in CVC bottle line operations can apply.

Zydus Lifesciences Warehouse Department: Plant Operator / Technical Assistant

Position Details

• Department: Warehouse
• Position: Plant Operator / Technical Assistant
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• ASRS
• Dispensing & Receipt

Eligibility & Qualifications

ITI | Diploma | B.Sc

Candidates with relevant experience in pharmaceutical warehouse operations, dispensing, receipt or ASRS activities can apply.

Zydus Lifesciences Warehouse Department: Officer / Senior Executive

Position Details

• Department: Warehouse
• Position: Officer / Senior Executive
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• ASRS
• Dispensing & Receipt

Eligibility & Qualifications

B.Sc | B.Pharm | Diploma | Graduate

Candidates with relevant warehouse experience involving ASRS, dispensing and receipt activities can apply.

Zydus Lifesciences Quality Control Department: Executive / Senior Executive

Position Details

• Department: Quality Control
• Position: Executive / Senior Executive
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• Analyst – Method Validation
• LC-MS
• Raw Material (RM)
• Finished Product (FP)
• Stability
• GLP

Eligibility & Qualifications

B.Sc | M.Sc | B.Pharm | M.Pharm

Candidates with relevant Quality Control experience in method validation, LC-MS, raw material, finished product, stability or GLP activities can apply.

Zydus Lifesciences Quality Assurance Department: Executive / Senior Executive

Position Details

• Department: Quality Assurance
• Position: Executive / Senior Executive
• Experience: 3–8 Years
• Work Location: SEZ-II Unit, Ahmedabad

Job Areas

• IPQA
• CSV
• OMS
• AQA
• Equipment & Utility Qualification
• Process Cleaning
• Whole Time Validation

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc | M.Sc

Candidates with relevant Quality Assurance experience in IPQA, CSV, OMS, AQA, qualification, process cleaning and validation activities can apply.

Zydus Lifesciences Recruitment: Eligibility & Qualifications

Eligible Qualifications

ITI | Diploma | B.Sc | M.Sc | B.Pharm | M.Pharm | B.E. | B.Tech

The required qualification varies according to the department and position.

Experience

3–8 Years

The recruitment is intended for experienced candidates with relevant pharmaceutical manufacturing, engineering, packing, warehouse, QC or QA experience.

Zydus Lifesciences Walk-In Interview Details

Walk-In Date

4 October 2026, Sunday

Walk-In Time

9:00 AM – 3:00 PM

Walk-In Venue

Papiya Tree Hotel
A. Mega City, Indore,
Madhya Pradesh – 453331

Work Location

Zydus Lifesciences Limited, SEZ-II Unit
Ahmedabad, Gujarat

Candidates attending the interview should apply for positions relevant to their qualification and experience.

How to Apply

Interested and eligible candidates can apply by scanning the QR code provided in the recruitment advertisement and submitting their application.

Candidates should ensure that their qualification and experience match the requirements of the position they wish to apply for.

Job Summary

Macleods Pharmaceuticals Ltd. is hiring an experienced professional for its Pharmacovigilance Department under the Safety Variations function.
The role is based in the company’s R&D function in Andheri, Mumbai, and requires experience in regulatory safety-related activities.
Candidates with 3–5 years of relevant experience in pharmacovigilance, regulatory safety variations, or related pharmaceutical functions can apply.
Eligible qualifications include M.Pharm, B.Pharm, BDS, and BHMS, while freshers are not eligible for this position.

Macleods Pharmaceuticals Pharmacovigilance Department: Safety Variations

Position Details

• Department: Pharmacovigilance
• Role: Safety Variations
• Function: R&D
• Experience: 3–5 Years
• Location: Andheri, Mumbai
• Qualification: M.Pharm / B.Pharm / BDS / BHMS

Eligibility & Qualifications

M.Pharm | B.Pharm | BDS | BHMS

Candidates should have 3–5 years of relevant experience. Freshers are not eligible for this role.

Macleods Pharmaceuticals Safety Variations: Roles & Responsibilities

SmPC & PIL Updates

• Update SmPC and PIL for Europe and the UK as per applicable requirements, including PRAC, CMDh, CHMP, Signal and other relevant regulatory requirements.
• Search regulatory websites for new updates from sources such as EMA, MHRA, EC decisions and HMA.

Regulatory & Interdepartmental Communication

• Coordinate with the Regulatory Affairs (RA) department regarding innovator information, common text and regulatory queries.
• Maintain effective interdepartmental communication for safety-related regulatory activities.

Regulatory Safety Monitoring

• Review and monitor regulatory updates related to safety changes.
• Identify relevant safety-related regulatory changes and assess their impact on product information.

Country-Specific Regulatory Review

• Search for country-specific innovator information and other relevant regulatory sources.
• Track applicable requirements for Europe and UK markets.

SmPC / PIL Review & RSI Updates

• Compare and review Europe and UK SmPC/PIL regularly as per the applicable SOP.
• Identify changes that need to be filed.
• Update the RSI and share the relevant information with the Regulatory Affairs team.

Macleods Pharmaceuticals Pharmacovigilance Role: Required Experience

Experience

3–5 Years

Candidates should have relevant experience in Pharmacovigilance, Safety Variations, regulatory safety activities, SmPC/PIL updates, or related pharmaceutical regulatory functions.

Freshers Eligibility

Freshers are not eligible for this position.

Macleods Pharmaceuticals R&D: Job Location

Work Location

Macleods Pharmaceuticals Ltd.
Andheri, Mumbai, Maharashtra

The position is part of the company’s R&D function and focuses on safety variations and regulatory activities for Europe and UK markets.

How to Apply

Interested and eligible candidates can share their updated resume with the recruitment contact:

Email: adityab@macleodspharma.com

Candidates should mention their relevant experience, current role and qualification clearly in their resume.

Important: Freshers should not apply for this role.

Jobs: Job Summary

Reliance Life Sciences is hiring freshers for opportunities in Plasma Proteins Manufacturing at its Navi Mumbai location.
The position is suitable for candidates with an M.Sc. qualification in Biotechnology, Microbiology, or Biochemistry.
This opportunity is intended for freshers interested in building a career in biopharma manufacturing.
Interested candidates can apply by sharing their updated resume with the recruitment team.

Reliance Life Sciences Plasma Proteins Manufacturing: Freshers

Position Details

• Department: Plasma Proteins Manufacturing
• Experience: Fresher
• Location: Navi Mumbai
• Qualification: M.Sc. in Biotechnology / Microbiology / Biochemistry

Eligibility & Qualifications

M.Sc Biotechnology | M.Sc Microbiology | M.Sc Biochemistry

Freshers with an M.Sc. qualification in Biotechnology, Microbiology, or Biochemistry are eligible to apply.

Reliance Life Sciences Biopharma Manufacturing: Career Opportunity

Role Overview

Selected candidates will have an opportunity to begin their career in Plasma Proteins Manufacturing and gain exposure to the biopharmaceutical manufacturing environment.

Experience

Freshers

No prior work experience is specified for this opportunity.

How to Apply for Reliance Life Sciences Recruitment

Interested candidates can share their updated resume with the recruitment team at:

Email: pradnya.kadu@relbio.com

Candidates should mention their relevant qualification and contact details clearly in the resume.

Job Summary

Tachyons Lifescience Pvt. Ltd. is hiring qualified professionals for multiple positions in its pharmaceutical formulation operations.
The current openings are available in Quality Assurance, Quality Control – Micro, and Business & Development.
Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc qualifications can apply for the relevant positions.
The company is looking for candidates with experience ranging from 6 months to 4 years, depending on the role.

Tachyons Lifescience Quality Assurance Department: Officer / Senior Officer

Position Details

• Department: Quality Assurance (QA)
• Position: Officer / Sr. Officer
• Qualification: B.Pharma / M.Pharma / B.Sc / M.Sc
• Experience: 2–4 Years
• Industry: Pharmaceutical Formulation

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc | M.Sc

Candidates with 2–4 years of relevant experience in the pharmaceutical formulation industry can apply for the Quality Assurance position.

Tachyons Lifescience Quality Control Department: Micro Officer / Executive

Position Details

• Department: Quality Control – Micro
• Position: Officer / Executive
• Qualification: B.Pharma / M.Pharma / B.Sc / M.Sc
• Experience: 2–4 Years
• Industry: Pharmaceutical Formulation

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc | M.Sc

Candidates with 2–4 years of relevant experience in pharmaceutical formulation can apply for the Quality Control – Micro position.

Tachyons Lifescience Business & Development Department: Officer

Position Details

• Department: Business & Development
• Position: Officer
• Qualification: B.Pharma / M.Pharma / B.Sc / M.Sc
• Experience: 6 Months–3 Years
• Industry: Pharmaceutical Formulation

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc | M.Sc

Candidates with 6 months to 3 years of relevant experience in the pharmaceutical formulation industry can apply.

Tachyons Lifescience Recruitment: Eligibility & Qualifications

Educational Qualifications

The recruitment notification lists the following qualifications:

B.Pharm | M.Pharm | B.Sc | M.Sc

Relevant pharmaceutical formulation experience is required for all three positions.

Experience Requirements

• Quality Assurance Officer / Senior Officer: 2–4 Years
• Quality Control – Micro Officer / Executive: 2–4 Years
• Business & Development Officer: 6 Months–3 Years

How to Apply

Interested candidates who meet the required qualifications and experience can apply by sending their updated CV to:

Email: recruitment@tachyonslifescience.com

Candidates should include the following information in their application:

• Total years of experience
• Current salary
• Expected salary
• Notice period
• Availability for a face-to-face interview
• Preferred interview date

WhatsApp Contact

WhatsApp: 90334 25045

Note: No calls on WhatsApp.

Candidates whose applications are shortlisted will be contacted by email or WhatsApp.

Job Summary

Cipla is conducting a walk-in interview for apprentice positions across its OSD Formulation, API Production, Engineering, Quality Control, and Quality Assurance functions.
The recruitment is open to freshers from relevant pharmacy, engineering, chemistry, and pharmaceutical backgrounds.
Candidates who completed their qualifying courses in the 2025–26 academic year can apply for the respective apprentice roles.
The walk-in interview will be held on 3 October 2026 from 9:00 AM to 1:00 PM at Cipla Ltd Unit 1, Patalaganga, Maharashtra.

Cipla OSD Formulation Production Department: Apprentice

Position Details

• Role: OSD Formulation Production
• Designation: Apprentice
• Experience: Fresher
• Qualification: Diploma in Pharmacy
• Passing Year: 2025–26

Job Description

• Operate and monitor OSD manufacturing operations as per SOPs.
• Maintain process parameters to ensure product quality.
• Perform equipment cleaning and changeover activities.
• Process data and maintain batch documentation.
• Follow GMP, safety, and other applicable requirements.

Eligibility & Qualifications

D.Pharm | Diploma in Pharmacy

Candidates who completed their Diploma in Pharmacy during 2025–26 and are interested in pharmaceutical formulation manufacturing can apply.

Cipla API Production Department: Apprentice

Position Details

• Role: API Production
• Designation: Apprentice
• Experience: Fresher
• Qualification: B.Sc Chemistry / Diploma Chemical
• Passing Year: 2025–26

Job Description

• Exposure to unit operations and unit processes of API manufacturing.
• Clean and maintain the equipment and ensure compliance with cGMP and safety requirements.
• Operate equipment such as reactors, centrifuges, filters, dryers, etc., involved in the production of APIs.
• Perform other responsibilities as per role requirements.

Eligibility & Qualifications

B.Sc Chemistry | Diploma Chemical

Candidates who completed the relevant qualification during 2025–26 can apply for this API Production apprentice opportunity.

Cipla Engineering Department: Apprentice

Position Details

• Role: Engineer
• Designation: Apprentice
• Experience: Fresher
• Qualification: Diploma Electrical / Mechanical / Instrumentation
• Passing Year: 2025–26

Job Description

• Support maintenance, troubleshooting, and operation of plant equipment and systems.
• Assist with preventive maintenance activities.
• Ensure smooth plant operations.
• Follow safety, GMP, and quality compliance requirements.
• Learn and gain hands-on experience in mechanical, electrical, and instrumentation functions.

Eligibility & Qualifications

Diploma Electrical | Diploma Mechanical | Diploma Instrumentation

Candidates who completed the relevant Diploma qualification during 2025–26 can apply.

Cipla Quality Control Department: Analyst Apprentice

Position Details

• Role: Analyst – Quality Control
• Designation: Apprentice
• Experience: Fresher
• Qualification: M.Sc Analytical Chemistry
• Passing Year: 2025–26

Job Description

• Perform chemical and physical analysis of raw materials, in-process samples, and finished products.
• Operate analytical instruments such as HPLC, GC, UV Spectrophotometer, FTIR, and Dissolution Apparatus.
• Prepare and maintain accurate records of test results and data analysis.
• Perform calibration and maintenance of analytical instruments.

Eligibility & Qualifications

M.Sc Analytical Chemistry

Candidates who completed their M.Sc in Analytical Chemistry during 2025–26 can apply for the Quality Control apprentice position.

Cipla Quality Assurance Department: Analyst Apprentice

Position Details

• Role: Analyst – Quality Assurance
• Designation: Apprentice
• Experience: Fresher
• Qualification: M.Sc Organic Chemistry
• Passing Year: 2025–26

Job Description

• Perform in-process checks during API manufacturing.
• Monitor critical process parameters and deviations.
• Ensure adherence to validated processes.

Eligibility & Qualifications

M.Sc Organic Chemistry

Candidates who completed their M.Sc in Organic Chemistry during 2025–26 can apply for the Quality Assurance apprentice position.

Cipla Apprentice Recruitment: Eligibility & Qualifications

The recruitment covers apprentice opportunities in OSD Formulation Production, API Production, Engineering, Quality Control, and Quality Assurance.

Eligible Qualifications

D.Pharm | B.Sc Chemistry | Diploma Chemical | Diploma Electrical | Diploma Mechanical | Diploma Instrumentation | M.Sc Analytical Chemistry | M.Sc Organic Chemistry

Experience

All positions shown in the recruitment notification are for freshers / apprentices.

Passing Year

The specified job qualifications are for candidates who completed their relevant course in the 2025–26 academic year.

Cipla Walk-In Interview Details

Interview Date

3 October 2026, Saturday

Interview Time

9:00 AM to 1:00 PM

Job Location

Patalaganga, Maharashtra

Interview Venue

Cipla Ltd Unit 1, Training Centre
MIDC Patalaganga, Tal. Khalapur,
Dist. Raigad – 410220, Maharashtra

How to Apply

Interested and eligible candidates should attend the walk-in interview at the specified venue on 3 October 2026 between 9:00 AM and 1:00 PM.

Candidates should carry the documents required for the recruitment process and verify their eligibility based on the qualification and passing-year requirements mentioned for the respective apprentice position.

The recruitment notification also asks candidates to scan the QR code provided in the official recruitment advertisement to apply.

Cipla Apprentice Recruitment: Important Notes

• The recruitment is for freshers.
• The applicable passing year mentioned is 2025–26.
• Candidates must meet the educational qualification specified for the respective role.
• The positions cover Production, Engineering, Quality Control, and Quality Assurance functions.
• The recruitment advertisement states that Cipla is looking for passionate individuals to join its purpose of “Caring for Life.”
• The advertisement also states that the company is shortlisting candidates based on its C&T and CoC process.

Job Summary

A pharmaceutical organization is hiring freshers for the position of Research Associate in its Formulation Department.
The role is suitable for candidates with a B.Pharm or M.Pharm in Pharmaceutics.
Selected candidates will support formulation development, pre-formulation studies, laboratory experiments, scale-up and technology transfer activities.
The interview is being conducted from 28 September to 5 October 2026, between 9:30 AM and 4:30 PM, at Tambaram, Tamil Nadu.

Formulation Department: Research Associate

Job Role

Research Associate – Formulation Department (Fresher)

Job Description

• Assist in formulation development of oral solid dosage forms, liquids, and injectables.
• Support pre-formulation studies and product optimization as per project requirements.
• Perform laboratory experiments and document the results.
• Maintain laboratory records and technical documentation.
• Assist in scale-up and technology transfer activities under guidance.
• Work with analytical, regulatory, and manufacturing teams.
• Ensure compliance with GMP and ICH guidelines.
• Support the department in achieving project timelines and development objectives.

Formulation Research Associate: Eligibility & Qualifications

Educational Qualification

B.Pharm in Pharmaceutics | M.Pharm in Pharmaceutics

Candidates with a B.Pharm or M.Pharm qualification in Pharmaceutics are eligible for this fresher position.

Experience

Fresher

No prior pharmaceutical industry experience is specified for this position.

Formulation Research Associate: Key Responsibilities

Formulation Development

The Research Associate will assist with formulation development activities covering oral solid dosage forms, liquids, and injectables.

Pre-Formulation & Product Optimization

The role involves supporting pre-formulation studies and product optimization according to project requirements.

Laboratory & Documentation

Candidates will perform laboratory experiments, document results, and maintain laboratory records and technical documentation.

Scale-Up & Technology Transfer

The selected candidate will assist in scale-up and technology transfer activities under appropriate guidance.

Cross-Functional Collaboration

The role requires coordination with analytical, regulatory, and manufacturing teams during formulation development activities.

GMP & ICH Compliance

Candidates will be expected to follow applicable GMP and ICH guidelines during laboratory and formulation development activities.

Formulation Research Associate: Interview Details

Interview Date

28 September 2026 to 5 October 2026

Interview Time

9:30 AM to 4:30 PM

Interview Address

Door No. 6, Kamarajar St,
East Tambaram, Selaiyur,
Tambaram, Tamil Nadu – 600059

Formulation Research Associate: Contact Details

HR Contact

Reyajitheen. A
Manager – HR

Mobile: +91 95001 12999
Email: hr@kmshc.com

How to Apply

Interested and eligible candidates can attend the interview between 28 September and 5 October 2026, from 9:30 AM to 4:30 PM, at the address mentioned above.

Candidates should carry an updated resume and relevant educational documents when attending the interview.

For recruitment-related queries, candidates can contact:

HR Email: hr@kmshc.com
Contact: +91 95001 12999

Job Summary