Author: Sudheer vanguri

Zenotech Laboratories Limited, a Sun Pharma company, is inviting applications for multiple positions in Quality Control (QC) and Quality Assurance (QA).
The openings include Senior Officer and Executive roles in Analysis-OSD, Analysis-General Injectable, QMS-General Injectable, and AQA-General Injectable.
Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and 2–8 years of relevant pharmaceutical industry experience can apply.
Interested applicants can submit their details through the online application form and email their resumes to the recruitment address provided below.

Company Overview

Zenotech Laboratories Limited is a pharmaceutical company associated with Sun Pharmaceutical Industries. The current recruitment drive covers Quality Control and Quality Assurance functions at its facility in Turkapally, Shameerpet, Medchal-Malkajgiri district, Telangana.

Zenotech Laboratories Department-Wise Vacancies

1. Senior Officer – Analysis-OSD

• Department: Quality Control
• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 2–4 years
• Key Responsibilities:

  • Operate, calibrate, and maintain GC, HPLC, and other analytical instruments.
  • Analyse raw materials and finished products.
  • Perform cleaning sample and stability sample analysis.

2. Senior Officer – Analysis-General Injectable

• Department: Quality Control
• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 2–4 years
• Key Responsibilities:

  • Operate, calibrate, and maintain GC, HPLC, and other analytical instruments.
  • Analyse raw materials and finished products.
  • Perform cleaning sample and stability sample analysis.

3. Senior Officer – QMS-General Injectable

• Department: Quality Assurance
• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 2–4 years
• Key Responsibilities:

  • Manage and monitor Quality Management System (QMS) activities, including change controls, deviations, CAPA, OOS, and product quality complaints.
  • Review, track, and ensure timely closure and effectiveness of CAPA and quality systems.
  • Control and maintain SOPs, protocols, training records, and EDMS documentation.
  • Support regulatory compliance, product recalls, audits, and continuous quality improvement.

4. Executive – QMS-General Injectable

• Department: Quality Assurance
• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 5–8 years
• Key Responsibilities:

  • Manage and monitor QMS activities, including change controls, deviations, CAPA, OOS, and product quality complaints.
  • Review, track, and ensure timely closure and effectiveness of CAPA and quality systems.
  • Control and maintain SOPs, protocols, training records, and EDMS documentation.
  • Support regulatory compliance, product recalls, audits, and continuous quality improvement.

5. Executive – AQA-General Injectable

• Department: Quality Assurance
• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 5–8 years
• Key Responsibilities:

  • Handle QMS activities such as change controls, deviations, CAPA, OOS, and PQC.
  • Manage SOPs, training records, and analytical documentation.
  • Ensure CAPA effectiveness, compliance, and regulatory readiness.
  • Support product recalls, audits, and continuous quality improvement.

Eligibility & Qualifications

Educational Qualifications

Candidates with any of the following qualifications may apply:

• B.Pharm
• M.Pharm
• M.Sc

Experience Requirements

• Senior Officer – Analysis-OSD: 2–4 years
• Senior Officer – Analysis-General Injectable: 2–4 years
• Senior Officer – QMS-General Injectable: 2–4 years
• Executive – QMS-General Injectable: 5–8 years
• Executive – AQA-General Injectable: 5–8 years

Required Skills

• Knowledge of analytical instruments such as GC and HPLC for Quality Control positions.
• Experience in raw material, finished product, cleaning sample, and stability sample analysis.
• Understanding of QMS processes, including change control, deviations, CAPA, OOS, and product quality complaints.
• Knowledge of SOP management, training documentation, and EDMS.
• Familiarity with pharmaceutical quality systems, regulatory compliance, audits, and continuous improvement.

Location & Salary

Job Location

Zenotech Laboratories Limited, Turkapally, Shameerpet, Medchal-Malkajgiri district, Telangana, India.

Salary Details

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

How to Apply

Interested candidates should complete the online application process and email their resumes to the recruitment contact.

Step 1: Complete the application form using the link below.

https://forms.office.com/r/Y5XKyCuUKKY

Step 2: Send your updated resume to:

Email: hr1@zenotech.co.in

Candidates should ensure that their contact details, qualifications, and relevant work experience are clearly mentioned in their resumes.

Important Instructions

• Apply for the position that matches your qualifications and experience.
• Provide accurate information in the application form.
• Highlight relevant pharmaceutical industry experience, particularly in analytical testing or quality systems, depending on the role.

Frequently Asked Questions

1. Which company is hiring for these positions?

Zenotech Laboratories Limited is recruiting for Quality Control and Quality Assurance roles.

2. What qualifications are accepted?

B.Pharm, M.Pharm, and M.Sc qualifications are listed in the recruitment announcement.

3. Can freshers apply?

The listed positions require 2–8 years of experience. Freshers are not eligible for these advertised vacancies based on the stated experience requirements.

4. What positions are available?

The vacancies include Senior Officer – Analysis-OSD, Senior Officer – Analysis-General Injectable, Senior Officer – QMS-General Injectable, Executive – QMS-General Injectable, and Executive – AQA-General Injectable.

5. Where is the job location?

The positions are based at Zenotech Laboratories Limited in Turkapally, Shameerpet, Medchal-Malkajgiri district, Telangana.

6. How can candidates apply?

Candidates can submit the online application form and email their resumes to hr1@zenotech.co.in.

Job Summary

Category	Details
Company	Zenotech Laboratories Limited
Vacancies	Senior Officer – Analysis-OSD; Senior Officer – Analysis-General Injectable; Senior Officer – QMS-General Injectable; Executive – QMS-General Injectable; Executive – AQA-General Injectable
Required Education	B.Pharm / M.Pharm / M.Sc
Experience	2–4 years for Senior Officer positions; 5–8 years for Executive positions

West Coast Pharmaceuticals Recruitment – FDA Assistant for Freshers

West Coast Pharmaceuticals is inviting applications for the FDA Assistant position at its facility in Sola, Ahmedabad, Gujarat. This opportunity is open to freshers who completed their education in 2026 or 2027. Candidates with B.Sc., M.Sc., or B.Pharm qualifications can apply for this entry-level pharmaceutical industry opportunity. Interested applicants can contact the recruitment team through WhatsApp or email their application directly to the company.

Company Overview

West Coast Pharmaceuticals is a pharmaceutical company offering career opportunities for candidates interested in the pharmaceutical industry. This recruitment drive is aimed at freshers seeking an FDA Assistant position in Ahmedabad.

Job Details

Eligibility & Qualifications

Candidates with the following qualifications can apply:

B.Sc., M.Sc., or B.Pharm.

• Eligible pass-out years: 2026 and 2027.

• Freshers are encouraged to apply.

Job Location & Working Schedule

• Location: Sola, Ahmedabad, Gujarat.

• Working hours: 9:00 AM to 7:00 PM.

• Working days: Monday to Saturday.

How to Apply

Interested candidates can apply directly through the company’s recruitment contact.

• Email: hrdho@westcoastin.com

• WhatsApp / Contact: +91 98751 70543

Applicants should mention FDA Assistant in their email subject line and include their updated resume.

Job Summary

Indero Recruitment – Senior Clinical Data Coder

Indero is inviting applications for the Senior Clinical Data Coder – India position on a permanent, full-time basis. This home-based opportunity is suitable for experienced professionals in clinical data coding, clinical trials, and pharmaceutical or contract research organization (CRO) environments. Candidates with at least five years of relevant experience, knowledge of MedDRA and WHO Drug dictionaries, and expertise in coding module setup can apply. The role involves clinical data coding, coding convention management, data review, query resolution, and coordination of coding activities across multiple studies.

Company Overview

Indero is a global contract research organization specializing in dermatology and rheumatology clinical research. Formerly known as Innovaderm, the company has more than two decades of clinical research experience and supports pharmaceutical and biotechnology sponsors through services spanning protocol design, patient recruitment, trial monitoring, and biometrics.

Indero emphasizes collaboration, innovation, reliability, and responsiveness, with opportunities for professional development and advancement.

Job Details

Job Role & Responsibilities

The Senior Clinical Data Coder will lead and oversee clinical data coding activities across multiple ongoing studies, ensuring coding accuracy, regulatory compliance, and timely delivery of study requirements.

Key responsibilities include:

• Code medical terms and medications accurately using MedDRA, WHO Drug, and internal coding conventions.

• Oversee coding module setup for assigned studies and ensure appropriate configurations and workflows.

• Define, document, and manage coding conventions to maintain consistency across studies.

• Coordinate coding activities as the Lead Coder across multiple studies simultaneously.

• Validate sponsor coding licenses.

• Prioritize coding deliverables and balance workloads across studies and timelines.

• Contribute to the coding sections of Data Management Plans.

• Oversee and perform dictionary version upgrades and related activities.

• Validate and test coding setups, coding report programming, and associated database checks.

• Support clinical data review and resolve data clarifications within required timelines.

• Mentor and guide junior or backup coders.

• Contribute to process optimization, SOP development, and coding best practices.

• Maintain effective communication with Data Management Leads, Clinical Research Associates (CRAs), and other stakeholders.

Eligibility & Qualifications

Candidates should possess a Bachelor’s degree or equivalent in Pharmacy, Life Sciences, or a related field. Medical or Nursing backgrounds are also acceptable.

Experience Requirements

• Minimum 5 years of relevant clinical data coding experience in clinical trials or the pharmaceutical/CRO environment.

• Demonstrated experience in coding module setup and coding convention management.

• Experience prioritizing coding tasks across multiple clinical studies.

• Experience in clinical data review and query management.

Required Skills & Competencies

Applicants should demonstrate the following skills and knowledge:

• Thorough knowledge of medical terminology.

• Working knowledge of MedDRA and WHO Drug medical dictionaries.

• Experience with coding module configuration, validation, and dictionary upgrades.

• Understanding of clinical data management workflows and coding-related database checks.

• Strong organizational, analytical, and problem-solving skills.

• High attention to detail and commitment to data accuracy.

• Excellent written and verbal English communication skills.

• Ability to lead and support colleagues in a global team environment.

• Good knowledge of Good Clinical Practice (GCP).

• Familiarity with applicable Health Canada, US FDA, and European Medicines Agency (EMA) regulations and guidelines.

Work Location & Benefits

This is a home-based position in India. Candidates should be legally eligible to work in India and willing to attend some meetings outside regular working hours, primarily in the evening.

Indero lists the following benefits:

• Flexible work schedule.

• Permanent, full-time employment.

• Ongoing learning and development opportunities.

• Opportunities for professional growth and advancement.

How to Apply

Interested and eligible candidates can submit their applications through the official Indero careers website.

Apply for Senior Clinical Data Coder – India

Applicants should review the official requirements and ensure they have the relevant clinical data coding experience, medical dictionary knowledge, and coding leadership capabilities.

Job Summary

Vantive Recruitment – Executive, Post Market Surveillance

Vantive is inviting applications for the Executive – Post Market Surveillance position in Gurgaon, Haryana. This opportunity falls under the Quality Product Surveillance category and focuses on medical device complaint handling, regulatory reporting, and post-market product monitoring. The role involves reviewing customer complaints, assessing reportability, preparing Medical Device Reports (MDRs), coordinating investigations, and ensuring timely complaint closure. Candidates interested in quality assurance, medical device safety, complaint management, and regulatory compliance can review the official job listing for eligibility details.

Company Overview

Vantive is a vital organ therapy company focused on extending lives and expanding possibilities for patients and healthcare teams. With a 70-year legacy in kidney care, the company is advancing dialysis services through digital solutions and advanced therapies while investing in the development of vital organ treatments.

Job Details

Job Role & Responsibilities

The Executive – Post Market Surveillance will manage and process product complaints and Medical Device Reports across multiple product lines, following applicable procedures and regulatory requirements.

Key responsibilities include:

• Open complaint records and collect the information required for complaint processing.

• Conduct written and verbal follow-ups with customers to obtain additional complaint details.

• Determine whether complaints meet regulatory reporting requirements.

• Prepare associated regulatory reports, including Medical Device Reports (MDRs), in accordance with applicable regulations.

• Evaluate complaints to determine whether an investigation is required.

• Coordinate the retrieval of product samples when necessary for investigations.

• Respond to customer complaints through written and verbal communication.

• Ensure timely closure of complaints in accordance with established procedures.

• Manage complaint-related workflows and identify issues requiring escalation.

• Triage internal and external communications related to product complaints.

• Participate in continuous improvement initiatives and assigned projects.

Eligibility & Qualifications

Pharmacy, Biomedical Engineering, Biotechnology, Life Sciences, and medical device quality or regulatory affairs.

Key Skills & Competencies

The responsibilities described in the listing indicate the importance of the following skills:

• Product complaint handling and documentation.

• Complaint reportability assessment.

• Medical Device Reporting (MDR) and regulatory documentation.

• Customer communication and follow-up.

• Complaint investigation coordination and sample retrieval.

• Workflow management and issue escalation.

• Compliance with established procedures.

• Quality improvement and cross-functional coordination.

Job Location

The position is based in Gurgaon, Haryana, India. The listing identifies the role under Quality Product Surveillance.

How to Apply

Interested candidates can review the official job description and submit their application through Vantive’s careers portal.

Apply for Executive – Post Market Surveillance

Applicants should verify the educational requirements, experience criteria, and other application details on the official portal.

Job Summary

Patanjali Research Foundation Recruitment – Scientific/Medical Writer

Patanjali Research Foundation is inviting applications for the Scientific/Medical Writer position in its Drug Discovery and Development Division. This opportunity is suitable for postgraduate and PhD candidates in Life Sciences, Biology, Chemistry, Pharmacy, Biotechnology, and related disciplines. Candidates with 2–4 years of experience in scientific manuscript writing, medical writing, or publication support are preferred, while freshers with strong subject knowledge may also be considered. The role involves scientific manuscript development, literature reviews, clinical research documentation, regulatory writing, and preparation of publication-ready research content.

Company Overview

Patanjali Research Foundation works in research and development across scientific disciplines. Its Drug Discovery and Development Division is seeking a scientific writing professional to support the Biology, Chemistry, and Clinical Research departments through scientific manuscripts, research documentation, and regulatory writing.

Job Details

Job Role & Responsibilities

The selected candidate will support scientific manuscript writing and documentation for Biology, Chemistry, and Clinical Research teams.

Key responsibilities include:

• Write, review, and edit scientific manuscripts for peer-reviewed journals in Biology, Chemistry, and Clinical Research.

• Develop review articles, research manuscripts, abstracts, posters, and conference presentations.

• Ensure manuscripts comply with journal-specific author guidelines and publication standards.

• Prepare literature reviews, study protocols, clinical study reports, regulatory documents, and project proposals.

• Collaborate with researchers to convert experimental, preclinical, and clinical data into publication-ready content.

• Conduct systematic literature reviews using recognized scientific databases.

• Analyze and interpret biological, chemical, and clinical datasets for accurate scientific representation.

• Perform quality checks for scientific accuracy, grammar, references, and formatting.

• Work with Biology, Chemistry, and Clinical Research teams, as well as project managers.

• Coordinate with internal and external stakeholders to support timely manuscript submission.

• Present complex experimental and clinical findings in clear, concise, scientifically accurate language.

• Adapt scientific content for researchers, clinicians, regulatory authorities, and peer reviewers.

• Use manuscript submission systems, reference management tools, and documentation software.

• Recommend improvements to scientific documentation quality and workflow efficiency.

Eligibility & Qualifications

Candidates should possess a Master’s degree or PhD in Life Sciences, Biology, Chemistry, Pharmacy, Biotechnology, or a related discipline.

Experience Requirements

• Preferred experience: 2–4 years.

• Freshers with strong subject knowledge may also be considered.

• Proven experience in manuscript writing or scientific/medical writing.

• Experience supporting publications in Biology, Chemistry, or Clinical Research is preferred.

Required Skills

Applicants should have the ability to:

• Write and edit scientific manuscripts with accuracy and clarity.

• Interpret scientific literature and research data.

• Prepare publication-ready documents in accordance with journal requirements.

• Conduct literature searches and systematic reviews.

• Manage references, citations, formatting, and manuscript submissions.

• Collaborate with multidisciplinary research teams.

• Communicate scientific findings effectively to different audiences.

• Maintain high standards of scientific accuracy and documentation quality.

Benefits

Patanjali Research Foundation lists the following benefits for this position:

• Competitive salary and benefits package.

• Opportunity to work in a collaborative research environment.

• Potential for professional growth and career advancement.

How to Apply

Interested candidates should apply by email with the required documents.

1. Prepare your detailed resume and cover letter, including your career aspirations.

2. Include three professional references who are not friends or family members.

3. Send your application to jobs@patanjali.res.in.

4. Mention Scientific/Medical Writing in the email subject line.

Application deadline: 28 February 2027

Official application details: Patanjali Research Foundation – Scientific/Medical Writer

Patanjali Research Foundation states that it is an equal opportunity employer and does not discriminate against applicants based on race, colour, religion, gender, national origin, age, or physical disability.

Job Summary

Worldwide Clinical Trials Recruitment – Senior Clinical Data Co-ordinator

Worldwide Clinical Trials is hiring a Senior Clinical Data Co-ordinator for its Clinical Data Management team in India. The full-time, on-site opportunity is available in Kochi and Trivandrum, Kerala. Candidates with at least five years of experience in data management systems and software, knowledge of CDISC SDTM standards, and SAS programming experience can apply. The role involves clinical database configuration, validation, SAS programming, data reconciliation, and coordination with sponsors and clinical data management teams.

Company Overview

Worldwide Clinical Trials is a global contract research organization (CRO) with more than 3,500 professionals working to support clinical research and improve patient outcomes. The company focuses on delivering clinical trial services through quality, innovation, collaboration, and scientific expertise.

Job Details

Job Role & Responsibilities

The Senior Clinical Data Co-ordinator will coordinate and perform activities related to the configuration, maintenance, and validation of clinical databases, database systems, and associated applications.

Key responsibilities include:

• Coordinate with relevant staff to allocate tasks, establish timelines, report progress, and communicate outstanding issues.

• Assist in training and mentoring Clinical Database Programmers in database configuration and SAS program development, testing, and execution.

• Support Data Management staff in preparing database and SAS program specifications.

• Review specifications for setting up and modifying project-specific data entry software, including edit checks.

• Review validation plans for edit checks and reconciliation checks.

• Develop, test, and run SAS programs for clinical data management, including data validation, reconciliation checks, data listings, and data transfers.

• Configure internal and third-party electronic data capture (eDC) and database software for Data Management teams, sponsors, and clinical sites.

• Test databases and related applications according to IT and Data Management departmental standard operating procedures (SOPs).

• Execute database upload programs and process error reports.

• Coordinate with third-party vendors to resolve issues and implement software changes.

• Communicate with sponsors or their representatives regarding electronic data transfers.

• Support the preparation and maintenance of system procedures and documentation in accordance with applicable SOPs.

• Assist with quality assurance activities and audit requirements.

• Perform other duties as assigned.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Education: Degree-level education or relevant experience.

• Experience: At least 5 years of experience working with data management systems and software.

• Clinical Data Standards: Understanding of CDISC SDTM standards.

• Programming Skills: Experience with the SAS programming language.

Required Skills & Competencies

Applicants should demonstrate the following skills:

• Good written and verbal communication skills.

• A methodical and logical approach to problem-solving.

• Ability to learn new tasks quickly and adapt to different computer systems.

• Strong attention to detail and a questioning approach to data validity.

• Good numerical and computer literacy.

• Ability to work efficiently and collaboratively.

• Customer focus and commitment to delivering on responsibilities.

• Relationship-building, communication, and influencing skills.

• Willingness to embrace innovation and organizational change.

Work Location

The position is listed as on-site and is available in:

• Kochi, Kerala

• Trivandrum, Kerala

This is a full-time opportunity with Worldwide Clinical Trials.

How to Apply

Interested and eligible candidates can apply through the official Worldwide Clinical Trials careers portal.

Apply for Senior Clinical Data Co-ordinator – Worldwide Clinical Trials

Applicants should review the official job description and ensure they meet the experience, CDISC SDTM, and SAS programming requirements before submitting their application.

Job Summary

NIPER Kolkata Recruitment – Junior Research Fellow (JRF)

The National Institute of Pharmaceutical Education and Research (NIPER), Kolkata, is inviting applications for one Junior Research Fellow (JRF) position under an Indian Council of Medical Research (ICMR)-sponsored research project. The opportunity is available in the Department of Medical Devices for research on bio-absorbable and antibiotic surgical staples used for wound closure. Candidates with an M.Pharm, M.S. (Pharm), M.Tech, M.Sc. in relevant scientific disciplines, or equivalent qualifications and at least 60% marks can apply. Applicants with experience in biomaterials development and a valid GPAT, NET, or GATE qualification will be preferred.

Organization Overview

The National Institute of Pharmaceutical Education and Research (NIPER), Kolkata, operates under the Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Government of India.

The institute is recruiting a Junior Research Fellow for a time-bound research project sponsored by the Indian Council of Medical Research (ICMR).

Project Title: Fiber Reinforced Poly (L–lactic acid) for Fabrication of Bio-absorbable and Antibiotic Surgical Staples for Wound Closing.

Job Details

Project Overview

The research project focuses on developing fiber-reinforced poly(L-lactic acid) materials for fabricating bio-absorbable and antibiotic surgical staples for wound closure.

The selected fellow will work within the Department of Medical Devices at NIPER Kolkata. Candidates with experience in biomaterials development are specifically sought for this research opportunity.

Eligibility & Qualifications

Candidates must possess one of the following qualifications, with a minimum of 60% marks in the degree:

M.Tech, M.S. (Pharm), M.Pharm, M.Sc. in Pharmacy, Biomedical Engineering, Biotechnology, M.Sc. in Chemistry, M.Sc. in Material Science, or an equivalent qualification.

The advertisement specifies that experience in biomaterials development is required.

Preferred Qualifications

• Valid GPAT, NET, or GATE qualification.

• Previous experience working on a funded research project.

Age Limit

The upper age limit is 28 years. Age relaxation for SC, ST, OBC, women, and persons with disabilities will be applicable according to Government of India rules.

Job Responsibilities & Research Focus

The project advertisement identifies biomaterials development as a key experience requirement. The research focuses on fiber-reinforced poly(L-lactic acid) for bio-absorbable and antibiotic surgical staples.

Specific day-to-day duties are not separately detailed in the supplied advertisement.

Fellowship & Contract Duration

The selected candidate will not be entitled to claim regular appointment or absorption at NIPER Kolkata on the basis of this fellowship.

Selection Process

• Applications will be reviewed, and candidates will be shortlisted.

• Shortlisted candidates will receive the interview date and time by email.

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

The advertisement does not specify a separate written examination.

How to Apply

Eligible Indian citizens should submit their application by email with the required documents combined into a single PDF file.

Email: nipercontrectt@niperkolkata.ac.in

CC: govinda@niperkolkata.ac.in

Email subject: Application for the post of JRF in Trachea Project

Documents Required

• Updated CV or resume.

• Attested copies of relevant educational certificates and mark sheets.

• Experience certificates, if applicable.

• Supporting documents relevant to the application.

Last date to apply: 17 October 2026. Applications received after the specified deadline may not be considered.

Official Links

• Download the official NIPER Kolkata JRF advertisement (PDF)

• Visit the NIPER Kolkata website

Important Instructions

• The position is purely contractual and time-bound.

• Fellowship continuation depends on satisfactory performance.

• Preference will be given to candidates with valid GPAT, NET, or GATE qualifications.

• Previous experience in a funded project is preferred.

• Canvassing in any form will result in disqualification.

• No TA/DA will be provided for the interview.

Job Summary

Indian Pharmacopoeia Commission Recruitment – Editorial Assistant

The Indian Pharmacopoeia Commission (IPC), under the Ministry of Health and Family Welfare, Government of India, is conducting a walk-in interview cum written test for the Editorial Assistant post at its Ghaziabad office. This opportunity is suitable for candidates with a postgraduate degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, Microbiology, Life Sciences, or a related scientific discipline. Applicants must have at least two years of relevant editorial experience, preferably in scientific, academic, pharmaceutical, or regulatory publications. The selected candidate will work on editing and proofreading Indian Pharmacopoeia monographs and related scientific publications under a one-year contract.

Organization Overview

The Indian Pharmacopoeia Commission is an autonomous organization under the Ministry of Health and Family Welfare, Government of India. It is responsible for publishing the Indian Pharmacopoeia and related publications.

The Editorial Assistant will support scientific publication quality through editing, proofreading, reference verification, documentation management, and coordination with authors, reviewers, and subject experts.

Job Details

Eligibility & Qualifications

Candidates must possess a master’s degree from a recognized university in one of the following disciplines:

M.Pharm, M.Sc. Chemistry, M.Sc. Biochemistry, M.Sc. Biotechnology, M.Sc. Microbiology, M.Sc. Life Sciences, or a related scientific discipline.

Experience Requirements

A minimum of 2 years of relevant experience is required in areas such as:

• Editorial work, preferably involving scientific, academic, pharmaceutical, or regulatory publications.

• Manuscript editing, proofreading, copyediting, and content review.

• Checking references, citations, bibliographies, appendices, addenda, and errata.

• Maintaining publisher-specific style guides and editorial standards.

• Publication workflows, documentation management, and version control.

• Coordinating with authors, reviewers, subject experts, and publishing teams.

Experience in government organizations, research institutions, pharmacopoeial bodies, scientific publishing houses, or scientific communication companies is desirable.

Job Role & Responsibilities

The selected candidate will support the editing, review, and publication of Indian Pharmacopoeia monographs and related publications.

Key responsibilities include:

1. Edit, proofread, and copyedit Indian Pharmacopoeia (IP) monographs, drafts, errata, addenda, IP Online content, and related publications.

2. Verify references, hyperlinks, citations, bibliographies, and appendices while maintaining IPC-specific editorial standards.

3. Manage documentation, version control, review tracking, and editorial records throughout publication workflows.

4. Coordinate with subject experts and reviewers to ensure timely content review, revision, and finalization.

5. Use MS Word, Excel, PowerPoint, PDF editing tools, AI tools, and editorial management systems to support editorial and publication-related activities.

Salary & Contract Details

The engagement is contractual. According to the vacancy circular, services may be terminated during the contract period if work or conduct is unsatisfactory.

Written Test Syllabus

Candidates should prepare the following subjects for the written test:

• English language: Grammar, comprehension, editing, proofreading, and copyediting.

• Scientific writing and publishing: Editorial practices, style guides, references, citations, bibliographies, appendices, errata, addenda, and publication ethics.

• Scientific knowledge: Basic pharmaceutical, chemical, biological, and life sciences concepts relevant to scientific and pharmacopoeial publications.

• Documentation and quality assurance: Documentation management, version control, editorial workflows, and quality assurance.

• Computer applications: MS Office, PDF editing tools, AI-assisted editing tools, and editorial management systems.

• Analytical ability: Scientific aptitude and analytical reasoning.

Walk-in Interview Details

Important: The walk-in interview cum written test will be conducted in physical mode only. No TA/DA will be paid for attending the selection process.

Documents Required

Candidates must bring the originals and self-attested photocopies of the required documents:

• Educational qualification certificates.

• Experience certificates.

• Updated resume.

• Two passport-size photographs.

• Aadhaar card (original).

• One set of photocopies of all original documents.

• Date of birth certificate.

Candidates should carry all relevant supporting documents for verification at the venue.

How to Apply

Eligible candidates should attend the walk-in interview cum written test at IPC, Ghaziabad, on 28 October 2026, reporting between 9:00 AM and 10:00 AM.

Read the official vacancy circular carefully before attending.

• Download the official IPC Editorial Assistant vacancy circular (PDF)

• Visit the official IPC Careers page

The selected candidate will be informed by the IPC-authorized manpower-providing agency. Candidates are responsible for ensuring that the information and documents submitted are correct.

Job Summary

DDReg Pharma Recruitment – Regulatory Affairs (Biologicals & Vaccines)

DDReg Pharma is hiring for the Senior Associate / Assistant Manager – Regulatory Affairs (Biologicals & Vaccines) position in Gurgaon, India. This opportunity is suitable for regulatory affairs professionals with 3–6 years of relevant experience in pharmaceutical regulatory submissions. The role focuses on preparing CTD/eCTD dossiers, managing CDSCO submissions, handling SUGAM portal activities, and supporting regulatory approvals for biological products and vaccines. Candidates with qualifications in Pharmacy, Life Sciences, Biotechnology, or related disciplines and hands-on regulatory submission experience can apply.

Company Overview

DDReg Pharma provides regulatory and pharmaceutical consulting services supporting regulatory projects across global markets. This position focuses on regulatory affairs activities related to biological products and vaccines, including dossier preparation, submission management, and regulatory compliance.

Job Details

Job Role & Responsibilities

The selected candidate will support regulatory submissions and compliance activities for biological products and vaccines in accordance with applicable Indian regulatory requirements.

Key responsibilities include:

• Prepare and submit Common Technical Document (CTD) and electronic Common Technical Document (eCTD) regulatory dossiers to the Central Drugs Standard Control Organisation (CDSCO).

• Manage clinical trial applications, licences, marketing authorisations, variations, and renewals.

• Handle submissions through the SUGAM portal and respond to regulatory queries.

• Ensure compliance with applicable CDSCO regulations, New Drugs and Clinical Trials Rules (NDCTR), and biologics guidelines.

• Coordinate regulatory activities with clients, internal teams, and regulatory authorities.

• Support documentation and submission processes to facilitate regulatory review and approvals.

Eligibility & Qualifications

Candidates should have a bachelor’s or master’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field.

Relevant qualifications include B.Pharm, M.Pharm, Pharm.D, B.Sc. Life Sciences, M.Sc. Life Sciences, B.Sc. Biotechnology, M.Sc. Biotechnology, or related scientific qualifications aligned with the employer’s stated requirements.

Experience Requirements

• 3–6 years of relevant Regulatory Affairs experience.

• Hands-on experience with CDSCO regulatory submissions.

• Practical experience preparing CTD/eCTD dossiers.

• Experience using the SUGAM portal for regulatory submissions.

• Understanding of applicable regulatory requirements for biological products and vaccines.

Required Skills

• Regulatory documentation and dossier preparation.

• Knowledge of CDSCO submission procedures and regulatory requirements.

• Familiarity with NDCTR and applicable biologics guidelines.

• Strong written and verbal communication skills.

• Stakeholder coordination and client communication.

• Ability to manage regulatory submissions and related documentation accurately.

Job Location & Work Environment

The position is based in Gurgaon, Haryana, and follows an office-based working arrangement. The role involves coordination with clients, internal departments, and regulatory authorities to support biologicals and vaccine regulatory projects.

How to Apply

Interested candidates can apply through the DDReg Pharma careers page or submit their CV directly by email.

• Careers page: Senior Associate / Assistant Manager – Regulatory Affairs

• Email: career@ddreg.in

• Company website: DDReg Pharma

Candidates should highlight their CDSCO submission experience, CTD/eCTD dossier preparation, and SUGAM portal expertise in their applications.

Job Summary

ALS Recruitment – Junior Chemist, HPLC Team

ALS Testing Services India Pvt. Ltd. is inviting applications for the Junior Chemist – HPLC Team position in Bengaluru, India. This opportunity is suitable for freshers and candidates with up to one year of testing laboratory experience. The role involves sample preparation, High-Performance Liquid Chromatography (HPLC) analysis, chromatogram review, quality control, and laboratory documentation. Candidates with a B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, Food Technology, Biotechnology, or a related scientific discipline can apply.

Company Overview

ALS is a global scientific testing company that provides laboratory testing services and data-driven insights across multiple industries. Its laboratory teams work to deliver reliable analytical results while maintaining quality, safety, and regulatory compliance.

Job Details

Job Role & Responsibilities

The selected candidate will perform sample preparation, chemical analysis, data processing, and documentation using HPLC and related analytical techniques.

Key responsibilities include:

• Prepare and analyse food, feed, water, environmental, and related samples using HPLC and associated techniques.

• Operate, calibrate, and maintain HPLC systems and supporting laboratory equipment according to approved procedures.

• Analyse vitamins, preservatives, sugars, organic acids, sweeteners, caffeine, colourants, and other chemical parameters within the laboratory’s testing scope.

• Review chromatograms, integration, calibration curves, and quality control data to verify the technical validity of results.

• Prepare and maintain analytical worksheets, test records, instrument logbooks, and laboratory documentation.

• Perform routine instrument suitability checks, preventive maintenance, and troubleshooting.

• Follow approved test methods, standard operating procedures (SOPs), ISO/IEC 17025 requirements, and ALS quality procedures.

• Meet sample throughput targets and agreed laboratory turnaround times.

• Participate in method verification, validation, measurement uncertainty studies, and proficiency testing programmes.

• Assist in investigating analytical deviations, out-of-specification results, and quality incidents under the guidance of the Team Leader.

• Maintain laboratory housekeeping, reagent preparation records, chemical inventory, and safety requirements.

• Support internal audits, NABL assessments, customer audits, and continuous improvement initiatives.

Eligibility & Qualifications

Candidates should have a B.Sc. or M.Sc. in Chemistry, Analytical Chemistry, Food Technology, Biotechnology, or a related scientific discipline.

Relevant courses include B.Sc. Chemistry, M.Sc. Chemistry, B.Sc. Analytical Chemistry, M.Sc. Analytical Chemistry, B.Sc. Food Technology, M.Sc. Food Technology, B.Sc. Biotechnology, and M.Sc. Biotechnology, subject to the employer’s stated qualification criteria.

Experience Requirements

• 0–1 year of experience in a testing laboratory.

• Freshers with academic or internship experience in HPLC techniques may also be considered.

• Experience in food testing laboratories is an added advantage.

Technical Skills & Knowledge

Candidates interested in this position should be familiar with or willing to develop skills in:

• High-Performance Liquid Chromatography (HPLC).

• Sample preparation and analytical testing.

• Chromatogram interpretation and calibration curves.

• Laboratory quality control and analytical documentation.

• Instrument calibration, maintenance, and troubleshooting.

• Standard operating procedures and laboratory safety.

• ISO/IEC 17025 laboratory quality requirements.

Work Location

The position is based at ALS Testing Services India Pvt. Ltd., Bengaluru, Karnataka. The role involves laboratory-based chemical testing and requires compliance with laboratory procedures, quality systems, safety requirements, and turnaround time commitments.

 

How to Apply

Interested candidates should apply online through the official ALS careers portal. Applicants should submit a resume and cover letter demonstrating their motivation and suitability for the position.

Apply here: Junior Chemist – HPLC Team | ALS Official Careers

Review the official job listing for the latest application status and eligibility requirements.

Job Summary