Job Tag: pharma jobs in hyderabad

Medical Writer Openings | MASUU Global Pharma | Hyderabad

MASUU Global hiring Medical Writers in Hyderabad. Vacancies for Executives (2–4 yrs) & Managers (8–10 yrs). Apply now! fapello angie wildernessbabe

MASUU Global Pharma, a leading Regulatory, Quality Services, and Software company, is hiring experienced Medical Writers for its Hyderabad office (Miyapur). This opportunity is open for both Managerial roles (8–10 years) and Executive roles (2–4 years) in medical writing. Please note, this is a full-time, on-site role (No WFH).

Company Overview

MASUU Global Pharma is an established global service provider specializing in pharmaceutical regulatory, quality, and technology solutions. With its expertise in supporting pharmaceutical, biotech, and healthcare companies across multiple regulatory landscapes, MASUU Global offers a dynamic work culture and opportunities to contribute to global drug development and compliance.

Job Role & Responsibilities

Position: Medical Writer (Executive / Manager)
Location: Hyderabad – Miyapur
Experience: Executive – 2–4 years | Manager – 8–10 years

Key Responsibilities:

• Prepare key regulatory and safety documents including:
  • CTD Module 2.5 (Clinical Overview) & Module 2.7 (Clinical Summary).
  • Risk Management Plans (RMP).
  • Initial Paediatric Study Plans (IPSP).
  • Study Protocols & Investigator Brochures (IB).
  • Investigational Medicinal Product Dossiers (IMPD).
  • Periodic Safety Update Reports (PSUR) and Periodic Benefit-Risk Evaluation Reports (PBRER).
• Draft and review pre-IND, IND, and scientific advice documents.
• Collaborate with cross-functional teams including Drug Safety Physicians, EU-QPPV, Risk Management, Clinical, PV, Regulatory, Legal, and Corporate Affairs.
• Provide medical writing expertise for regulatory interactions (Type A, B, and C meetings).
• Ensure compliance with ICH and global regulatory standards.
• Perform quality control, validation, and adherence to client-specific templates.

Eligibility / Qualifications

• Education: Life Sciences / Pharmacy / Medicine / Clinical Research (B.Pharm, M.Pharm, Pharm.D, MBBS, MSc, PhD preferred).
• Experience: 2–4 years (Executive) or 8–10 years (Manager) in medical writing or regulatory writing.
• Skills Required:
  • Strong knowledge of clinical and regulatory documentation.
  • Familiarity with ICH, EMA, USFDA, and global regulatory requirements.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple projects and meet deadlines.

Location & Salary

• Work Location: MASUU Global Pharma, Miyapur, Hyderabad.
• Job Type: Full-time (No WFH option).
• Salary: Competitive, based on qualifications and experience.

Application Process

Candidates interested in applying should send their CVs to:

• Email: hiring@masuuglobal.com
• Call/WhatsApp: +91 9154979318
• Subject Line: CV for Medical Writer
• Website: www.masuuglobal.com

Applicants are encouraged to apply early to secure their role in this hiring drive.

FAQs

1. Who can apply for MASUU Global’s Medical Writer role?
Life Sciences, Pharmacy, and Clinical Research professionals with 2–10 years of medical writing experience.

2. What are the available levels of hiring?
Executive (2–4 years’ experience) and Manager (8–10 years’ experience).

3. Is remote work allowed?
No, this is a full-time on-site position in Hyderabad (Miyapur).

4. What types of documents will I work on?
Regulatory, clinical, and safety documents including CTD modules, RMP, IMPD, PSUR, PBRER, and study protocols.

5. How can I apply?
Email your CV to hiring@masuuglobal.com with the subject line “CV for Medical Writer” or contact via WhatsApp at 9154979318.

Apply now and join MASUU Global Pharma in Hyderabad as a Medical Writer to advance your career in regulatory and scientific writing!

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Bioprocess Production Vacancies | Bharat Biotech | Hyderabad

Bharat Biotech hiring Bioprocess Production (Upstream & Downstream) in Hyderabad. B.Sc/M.Sc/B.Tech with 3–8 years’ vaccine/biopharma experience.

Bharat Biotech International Ltd., a pioneer in vaccine innovation and manufacturing, is inviting applications for its Bioprocess Production Team (Upstream & Downstream) at Genome Valley, Hyderabad. This opportunity is ideal for experienced professionals with a background in bacterial vaccine or biopharma production.

Company Overview

Bharat Biotech International Limited is globally recognized for its contributions to vaccine research, development, and large-scale manufacturing. With a portfolio that includes life-saving vaccines such as Covaxin and several WHO-prequalified products, the company has established itself as a leader in global healthcare. Headquartered in Hyderabad’s Genome Valley, Bharat Biotech offers a world-class facility, compliance with international regulatory standards, and opportunities for professionals to work on cutting-edge biopharmaceutical processes.

Job Role & Responsibilities

Position: Bioprocess Production – Upstream & Downstream (Bacterial Vaccine Production)
Experience Required: 3–8 years

Upstream Production Responsibilities

• Operation of bioreactors, fermenters, and incubators.
• Media preparation and cell culture handling.
• Monitoring critical parameters: pH, dissolved oxygen, temperature, agitation, etc.

Downstream Production Responsibilities

• Operation of centrifuges, TFF systems, chromatography skids, and filtration units.
• Execution of purification processes such as affinity and ion-exchange chromatography.
• Preparation of buffers and CIP/SIP of production equipment.

General Responsibilities

• Ensure adherence to GMP, GDP, SOPs, and safety protocols.
• Documentation and reporting of process parameters and deviations.
• Work in controlled cleanroom environments and support cross-functional teams.

Eligibility / Qualifications

• Education: B.Sc / M.Sc / B.Tech in Biotechnology, Microbiology, Biochemistry, or related fields.
• Experience: 3–8 years in vaccine or biopharma production (upstream/downstream).
• Skills Required:
  • Strong understanding of upstream fermentation and downstream purification.
  • Hands-on experience with cleanroom operations and GMP compliance.
  • Ability to work in rotational shifts.

Location & Salary

• Work Location: Genome Valley, Hyderabad
• Job Type: Full-time
• Salary: Competitive; based on qualifications and experience.

Application Process

Interested candidates can share their resumes to:

• Email: kiran4978@bharatbiotech.com

Suitable candidates will be contacted by the recruitment team for further evaluation.

FAQs

1. Who can apply for this role at Bharat Biotech?
Candidates with 3–8 years of experience in vaccine or biopharma production and qualifications in biotechnology, microbiology, or related fields.

2. What are the main responsibilities?
Managing upstream (bioreactors, fermenters, cell culture) and downstream (chromatography, filtration, purification) processes in bacterial vaccine production.

3. Is prior vaccine industry experience mandatory?
Yes, hands-on experience in vaccine or biopharma production is required.

4. Where is the role located?
At Bharat Biotech’s state-of-the-art manufacturing facility in Genome Valley, Hyderabad.

5. What is the application process?
Send your CV directly to kiran4978@bharatbiotech.com with relevant details.

Apply today and become part of Bharat Biotech’s mission to deliver world-class vaccines and biopharma products that save lives globally!

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Ciron Pharma Hiring | Procurement, Regulatory Affairs, Project Mgmt | Mumbai

Ciron Drugs & Pharmaceuticals hiring in Procurement, Regulatory Affairs (ROW), and Project Management. Apply now in Mumbai!

Ciron Drugs & Pharmaceuticals Pvt. Ltd., a globally recognized pharmaceutical formulation manufacturer and leading exporter of generics and branded medicines, is hiring for multiple roles in Procurement, Regulatory Affairs, and Project Management. This is an excellent opportunity for professionals looking to work in a reputed organization with a strong international presence.

Company Overview

Ciron Drugs & Pharmaceuticals is one of India’s leading pharma companies, known for its state-of-the-art manufacturing facilities, regulatory approvals, and strong global footprint. With exports across regulated and semi-regulated markets, the company is committed to delivering affordable, high-quality medicines. Ciron offers a dynamic work culture, growth opportunities, and exposure to international business practices.

Job Role & Responsibilities

1. Sourcing / Procurement Officer / Executive (2 Vacancies)

• Experience: 2–5 years
• Responsibilities:
  • Vendor management and raw material sourcing.
  • Negotiating contracts and maintaining supplier relationships.
  • Ensuring cost efficiency and timely procurement for smooth operations.

2. Regulatory Affairs – Officer / Executive (5 Vacancies)

• Focus: ROW (Rest of the World) Markets
• Experience: 1–5 years
• Responsibilities:
  • Preparation, review, and submission of regulatory dossiers for ROW markets.
  • Handling regulatory queries and supporting product registrations.
  • Ensuring compliance with international regulatory standards.

3. Project Management Executive (1 Vacancy)

• Experience: 5–7 years
• Responsibilities:
  • Oversee pharmaceutical project planning and execution.
  • Coordinate with cross-functional teams for timely delivery.
  • Ensure compliance with regulatory and quality standards throughout the project lifecycle.

Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, M.Sc, MBA (preferred for procurement & project management).
• Experience: 1–7 years depending on the role.
• Skills Required: Regulatory compliance knowledge, vendor negotiation, project management expertise, communication skills.

Location & Salary

• Job Location: Mumbai (Head Office – Ciron Drugs & Pharmaceuticals Pvt. Ltd.)
• Job Type: Full-time
• Salary: Competitive; based on qualifications and experience.

Application Process

Interested candidates can apply by sending their updated CV to:

• Email: hr.ho@cironpharma.com
• Website: www.cironpharma.com

FAQs

1. Who can apply for these Ciron Pharma openings?
Candidates with pharma/life sciences/business backgrounds and relevant industry experience can apply.

2. How many vacancies are available?
There are 8 vacancies across Procurement (2), Regulatory Affairs (5), and Project Management (1).

3. Is regulatory affairs experience specific to any market?
Yes, candidates must have experience in ROW (Rest of the World) markets regulatory submissions.

4. What is the work location?
All positions are based at Ciron’s Head Office in Mumbai.

5. How can I apply?
Send your updated resume to hr.ho@cironpharma.com or visit the company’s official website.

Apply now to join Ciron Pharma and build a rewarding career in Procurement, Regulatory Affairs, or Project Management at Mumbai!

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IPQA Executive & Sr. Executive Vacancies | Aurobindo Pharma Unit 7

Aurobindo Pharma Unit 7 hiring 10–20 IPQA Executives/Sr. Executives. B.Pharm/M.Pharm/M.Sc with 3–9 years’ experience. Apply now!

Aurobindo Pharma Ltd., one of India’s largest pharmaceutical companies, is hiring Executives and Senior Executives for its IPQA (In-Process Quality Assurance) department at Unit 7 – Jadcherla. This is an excellent opportunity for qualified pharma professionals to contribute to quality excellence in a company that has a global presence in formulations and active pharmaceutical ingredients.

Company Overview

Aurobindo Pharma Ltd. is a multinational pharmaceutical company headquartered in Hyderabad, India. It is among the top global producers of generic medicines, exporting to over 150 countries. Known for its expertise in Oral Solid Dosage (OSD), Dermatology, and Transdermal formulations, Aurobindo is driven by innovation, regulatory compliance, and patient safety. The company offers a professional work environment with opportunities for career growth and skill enhancement.

Job Role & Responsibilities

Position: Executive / Sr. Executive – IPQA (OSD / Derma / Trans-Derma)
Vacancies: 10–20

Key Responsibilities:

• Perform in-process quality assurance checks in manufacturing of OSD, Derma, and Transdermal products.
• Monitor adherence to GMP, SOPs, and regulatory compliance during production.
• Review and verify batch manufacturing records, logbooks, and documentation.
• Ensure compliance with quality systems and perform line clearance activities.
• Collaborate with production and quality control teams for deviation handling and CAPA implementation.
• Support audits and inspections by regulatory authorities.

Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, or M.Sc (Pharmaceutical Sciences, Chemistry, Life Sciences).
• Experience: 3–9 years in IPQA, quality assurance, or formulation manufacturing (OSD/Derma/Transderma).
• Skills Required: Strong knowledge of GMP, QMS, regulatory requirements, and pharmaceutical documentation.

Location & Salary

• Work Location: Unit 7 – Jadcherla, India
• Job Type: Full-time
• Salary: Competitive; based on qualifications and experience.

Application Process

Interested candidates should send their updated CV to:

• Email: hrsez@aurobindo.com

Subject Line: Application for IPQA

Applicants must mention the following details in the email body:

• Current CTC
• Expected CTC
• Notice Period

FAQs

1. Who can apply for Aurobindo Pharma’s IPQA vacancies?
Candidates with B.Pharm, M.Pharm, or M.Sc degrees and 3–9 years of experience in IPQA or related QA functions can apply.

2. How many vacancies are available?
There are 10–20 openings for Executive and Sr. Executive positions.

3. What departments are these roles associated with?
The positions are in In-Process Quality Assurance (IPQA) for OSD, Derma, and Trans-Derma products.

4. What is the application deadline?
Applications are open now. It is advised to apply at the earliest as shortlisting will be on a rolling basis.

5. What is the work location?
Unit 7 – Jadcherla, a key Aurobindo Pharma manufacturing site.

Apply now to join Aurobindo Pharma’s IPQA team and contribute to global pharmaceutical quality standards!

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FRD Scientist & Sr. Research Associate | M.Pharm | Novich Biosciences Balanagar

Apply for FRD Scientist & Sr. Research Associate at Novich Biosciences, Balanagar. M.Pharm with 6–10 years’ experience in OSD & solutions.

Novich Biosciences is expanding its Formulation Research & Development (FRD) team and is currently hiring for the positions of FRD Scientist and FRD Senior Research Associate at its Balanagar location. This opportunity is ideal for M.Pharm (Pharmaceuticals) professionals with hands-on experience in Oral Solid Dosage (OSD) and Solutions. If you are passionate about research, product development, and innovation in pharmaceuticals, this is your chance to join a growing biosciences company.

Company Overview

Novich Biosciences is a reputed name in the pharmaceutical research and development sector. With a strong emphasis on formulation innovation, quality, and regulatory compliance, the company develops advanced drug delivery systems and novel formulations. Novich fosters a collaborative work culture and provides a platform for professionals to contribute toward improving healthcare through innovative formulations.

Job Role & Responsibilities

FRD Scientist

• Qualification: M.Pharm (Pharmaceuticals)
• Experience: 8–10 years (OSD & Solutions)
• Key Responsibilities:
  • Coordinate with the analytical team to plan product development and sample submissions.
  • Lead end-to-end product development of oral solid dosages and solutions.
  • Design and execute pharmaceutical development experiments, including pre-formulation trials, development batches, compatibility studies, and stability testing.
  • Optimize processes and finalize critical parameters using Quality by Design (QbD) principles.
  • Collaborate in fast-paced multidisciplinary teams for screening and characterization strategies.
  • Ensure effective communication, documentation, and regulatory compliance.

FRD Senior Research Associate

• Qualification: M.Pharm (Pharmaceuticals)
• Experience: 6–7 years (OSD & Solutions)
• Key Responsibilities:
  • Conduct product development activities for tablets and solutions.
  • Prepare detailed project documentation in compliance with GMP guidelines.
  • Operate and maintain lab equipment such as blenders, granulators, mixers, and coating machines.
  • Maintain lab notebooks with accurate observations, ensuring compliance with GLP practices.
  • Prepare formulation sheets, Batch Manufacturing Records (BMR), and SOPs.

Note: Preference will be given to male candidates as per project requirements.

Eligibility / Qualifications

• Education: M.Pharm (Pharmaceuticals).
• Experience: 6–10 years in FRD (OSD & Solutions).
• Skills Required: Product development expertise, GMP/GLP knowledge, QbD exposure, documentation, equipment handling, and teamwork.

Location & Salary

• Location: Balanagar, India
• Job Type: Full-time
• Salary: Competitive, based on experience and qualifications.

Application Process

Interested candidates should submit their updated resume to:

• Email: recruitment@novickbio.com
• Application Dates: 21st August 2025 – 31st August 2025

Applicants are encouraged to apply early as shortlisting will be done on a rolling basis.

FAQs

1. Who can apply for Novich Biosciences FRD roles?
Candidates with an M.Pharm (Pharmaceuticals) degree and 6–10 years of experience in OSD and solutions can apply.

2. Are freshers eligible for these positions?
No, these roles require prior industry experience in formulation research and development.

3. What are the skills required for FRD Scientist and Sr. Research Associate?
Hands-on knowledge in OSD & solution development, QbD, GMP/GLP compliance, and equipment handling are essential.

4. Where is the job location?
The positions are based at Novich Biosciences, Balanagar, India.

5. What is the last date to apply?
The last date to apply is 31st August 2025.

Apply before 31st August 2025 to join Novich Biosciences’ FRD team and advance your career in pharmaceutical research!

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