Author: Sudheer vanguri

BDR Pharmaceuticals Walk-In Drive 2026: Production, QC, QA, R&D and Regulatory Affairs Jobs

BDR Pharmaceuticals International Pvt. Ltd. is conducting a walk-in recruitment drive for experienced professionals across multiple pharmaceutical departments.
The openings cover Analytical Method Validation and Development, Production, Quality Control, Regulatory Affairs, Research and Development, Engineering, Human Resources, Warehouse and Quality Assurance.
Candidates with relevant pharmaceutical qualifications and industry experience can apply for positions in the OSD and API divisions.
The walk-in interview is scheduled for 24 October 2026, from 10:00 AM to 4:00 PM, at BDR Pharmaceuticals International Private Limited, Luna, Padra, Gujarat.

BDR Pharmaceuticals Recruitment: Company Overview

BDR Pharmaceuticals International Pvt. Ltd. is inviting experienced candidates to explore opportunities in pharmaceutical manufacturing, analytical development, quality systems, regulatory affairs, and support functions. The recruitment drive includes openings for officers, executives, senior officers, assistant managers, and specialized professionals.

BDR Pharmaceuticals Walk-In Drive: Department-Wise Vacancies

1. Analytical Method Validation and Development

Division: OSD / API

Available Positions and Requirements:

• HPLC Analyst, Query Response, Officer to Executive
• Reviewer, HPLC, GC, Query Response, Senior Executive to Assistant Manager
• User Analyst, LCMS and GCMS, Officer to Executive
• User Analyst, XRD and ICPS, Officer to Senior Officer
• Reviewer, XRD, LCMS, ICPMS and GCMS, Executive to Assistant Manager
• QA, AMV, AMT, Compliance and Documentation, Officer to Executive

2. Production

Division: API

Available Positions and Requirements:

• Assistant Manager: Minimum 12 years of experience in production planning, equipment occupancy, troubleshooting, and root cause analysis. Experience in MS is required.
• Executive: 6+ years of experience. Shift in-charge and spray dryer experience are required.
• Officer / Senior Officer: 4–5 years of experience. Spray dryer experience is required.

3. Quality Control (QC)

Division: OSD

• Position: Officer to Senior Officer
• Specialization: HPLC
• Qualification: B.Sc, M.Sc, or B.Pharm

4. Regulatory Affairs

Division: API

• Position: Executive / Senior Executive
• Experience: 5–7 years

5. Research and Development (R&D)

Division: API

• Position: Officer
• Experience: 2–5 years
• Qualification: M.Sc in Organic Chemistry
• Areas of Work: Polymorphism, peptides, LCMS, and synthesis

6. Engineering

Division: API

Available Positions:

• Senior Officer / Executive – HVAC, RO, utilities, and building maintenance
• Senior Officer / Executive – QMS and documentation

7. Human Resources – Talent Acquisition

• Position: Talent Acquisition Specialist
• Experience: 2–3 years
• Preference: Pharmaceutical hiring exposure is preferred.

8. Warehouse / Stores

Division: API

• Position: Senior Officer
• Experience: 4–6 years

9. Quality Assurance (QA)

Division: OSD

• Position: Assistant Manager
• Experience: 10+ years

Eligibility & Qualifications

The recruitment announcement specifies qualifications for selected positions, including:

• B.Sc
• M.Sc
• B.Pharm
• M.Sc in Organic Chemistry

Candidates should review the individual position requirements and ensure their qualifications and experience match the department they wish to join. The advertisement does not specify educational qualifications for every position.

BDR Pharmaceuticals Walk-In Interview Details

Date and Time

• Date: Saturday, 24 October 2026
• Time: 10:00 AM to 4:00 PM

Interview Venue

BDR Pharmaceuticals International Private Limited

Luna, Padra, Gujarat.

How to Apply for BDR Pharmaceuticals Recruitment

Interested candidates can contact the recruitment representatives listed in the announcement for further information about the relevant vacancies.

API Division Contacts

• Kush Dave: kush.dave@bdrpharma.com
• Vidhi Machhi: vidhi.machhi@bdrpharma.com

OSD Division Contact

• Pritam Singha: pritam.singha@bdrpharma.com

Candidates should share an updated resume highlighting their relevant pharmaceutical industry experience, qualifications, and current designation.

Documents to Keep Ready

• Updated resume or CV
• Educational certificates
• Relevant experience certificates
• Employment details and supporting documents

Frequently Asked Questions

1. When is the BDR Pharmaceuticals walk-in interview?

The walk-in drive is scheduled for 24 October 2026, from 10:00 AM to 4:00 PM.

2. Where is the interview venue?

The interview will be held at BDR Pharmaceuticals International Private Limited, Luna, Padra, Gujarat.

3. Which departments have vacancies?

The openings cover Analytical Method Validation and Development, Production, Quality Control, Regulatory Affairs, R&D, Engineering, Human Resources, Warehouse / Stores, and Quality Assurance.

4. What qualifications are required?

The announcement lists B.Sc, M.Sc, B.Pharm, and M.Sc in Organic Chemistry for selected positions. Requirements vary by role.

5. How much experience is required?

Experience requirements vary by position, from 2–3 years for Talent Acquisition Specialist to 10+ years for Assistant Manager in Quality Assurance and a minimum of 12 years for Assistant Manager in Production.

6. How can candidates contact the recruitment team?

Candidates can email the listed recruitment contacts for the API and OSD divisions.

Job Summary

Category	Details
Company	BDR Pharmaceuticals International Pvt. Ltd.
Vacancies	Analytical Method Validation and Development, Production, QC, Regulatory Affairs, R&D, Engineering, Talent Acquisition, Warehouse / Stores, QA
Required Education	B.Sc, M.Sc, B.Pharm, M.Sc in Organic Chemistry; role-specific requirements apply
Experience	Varies by position; approximately 2–12+ years

 

Sudeep Nutrition Recruitment 2026 – Production Supervisor & Plant Operator

Sudeep Nutrition Pvt. Ltd. is hiring Production Supervisors and Plant Operators for its manufacturing facility in Vadodara, Gujarat. These production jobs are suitable for qualified candidates with experience in pharmaceutical, chemical, nutrition ingredient, or related manufacturing operations. Applicants with backgrounds in B.Sc., M.Sc., Pharmacy, ITI (AOCP), or Chemical Diploma programs can check the role-specific requirements below. The positions are based at Poicha (Rania), Taluka Savli, Vadodara, and require rotational shift work.

Company Overview

Sudeep Nutrition Pvt. Ltd. is recruiting professionals to support its nutrition ingredient manufacturing operations. The company is seeking candidates who can operate production equipment, maintain manufacturing documentation, follow Good Manufacturing Practices (GMP), and meet production schedules.

Job Details

1. Production Supervisor

Experience: 2–5 years

Qualification: B.Sc. / M.Sc. / B.Pharm. / M.Pharm.

Job Responsibilities

• Handle production equipment, including sifters, Fluid Bed Dryers (FBD), dryers, centrifuges, ANF equipment, and granulation equipment.

• Ensure compliance with Good Manufacturing Practices (GMP).

• Maintain Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and logbooks.

• Follow the production plan and support timely execution of manufacturing activities.

2. Plant Operator

Experience: Minimum 1 year

Qualification: ITI (AOCP) or Diploma in Chemical Engineering.

Job Responsibilities

• Operate production equipment, including sifters, Rapid Mixer Granulators (RMG), cone mills, Fluid Bed Dryers (FBD), Fluid Bed Coaters (FBC), roll compactors, oscillating granulators, and blenders.

• Follow GMP requirements and workplace safety practices.

• Maintain BMR, BPR, and logbooks.

• Follow the production plan and support routine manufacturing operations.

Eligibility & Qualifications

Candidates should meet the educational and experience requirements specified for their chosen position.

• Production Supervisor: B.Sc., M.Sc., B.Pharm., or M.Pharm., with 2–5 years of experience.

• Plant Operator: ITI (AOCP) or Diploma in Chemical Engineering, with at least 1 year of experience.

Candidates should be familiar with the relevant production equipment, manufacturing documentation, and GMP practices applicable to their role.

Important Note

Candidates selected for these positions will be required to work in rotational shifts.

Job Location

Poicha (Rania), Taluka Savli, Vadodara, Gujarat, India.

How to Apply

Interested candidates can apply online using the application form shared in the company’s recruitment announcement.

Apply Online – Sudeep Nutrition Recruitment

Applicants should select the appropriate position and provide accurate information about their qualifications and experience.

Job Summary

Almon Healthcare Pvt. Ltd. Recruitment 2026: Production, QC, QA, QMS and Regulatory Affairs Jobs

Almon Healthcare Pvt. Ltd. is inviting applications for multiple positions at its API manufacturing plant in Gujarat.
The company has openings in Production-QMS, QC-ADL, Quality Control, Quality Management System, Regulatory Affairs, and QA-Analytical departments.
Candidates with B.Sc, M.Sc, B.Pharm, or M.Pharm qualifications and relevant pharmaceutical industry experience can apply for suitable positions.
The recruitment drive includes 28 vacancies, with a face-to-face interview process at Kerala GIDC, Bavla, Ahmedabad, Gujarat.

Almon Healthcare Pvt. Ltd. Recruitment: Company Overview

Almon Healthcare Pvt. Ltd. is recruiting professionals for its API manufacturing plant. The current hiring drive covers production, analytical development, quality control, quality management systems, regulatory affairs, and analytical quality assurance.

Almon Healthcare Recruitment: Department-Wise Vacancies

1. Production – QMS

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 5–7 years
• Number of Vacancies: 2

Candidates with relevant pharmaceutical manufacturing and Quality Management System (QMS) experience can apply for this position.

2. QC – ADL

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 4 years
• Number of Vacancies: 5

This position is suitable for candidates with relevant experience in Quality Control and Analytical Development Laboratory (ADL) operations.

3. Quality Control (QC)

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 4–6 years
• Number of Vacancies: 8

Candidates with pharmaceutical quality control experience can apply for the available QC positions.

4. Quality Management System (QMS)

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 4 years
• Number of Vacancies: 5

Applicants with experience in pharmaceutical quality systems and related documentation can consider these openings.

5. Regulatory Affairs (RA)

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 3+ years
• Number of Vacancies: 4

This opportunity is intended for candidates with relevant experience in pharmaceutical regulatory affairs.

6. QA – Analytical

• Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
• Experience: 4–6 years
• Number of Vacancies: 4

Candidates with relevant analytical quality assurance experience can apply for these positions.

Eligibility & Qualifications

The recruitment announcement lists the following educational qualifications across the advertised departments:

• B.Sc
• M.Sc
• B.Pharm
• M.Pharm

Experience requirements vary by department, ranging from 3+ years in Regulatory Affairs to 5–7 years in Production-QMS.

Candidates should apply for positions matching their qualifications and relevant pharmaceutical industry experience.

Job Location and Interview Process

Work Location: Almon Healthcare Pvt. Ltd., Kerala GIDC, Bavla, Ahmedabad, Gujarat.

Interview Mode: Face-to-face interview.

Transportation: AC staff bus transportation is available from Ahmedabad, according to the recruitment announcement.

How to Apply for Almon Healthcare Recruitment

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

Email: hr.almonhc@gmail.com

Candidates should mention their preferred department and relevant experience when submitting their resumes. Applicants should confirm interview scheduling and any additional instructions with the recruitment team before attending.

Frequently Asked Questions

1. Which company is hiring?

Almon Healthcare Pvt. Ltd. is recruiting for its API manufacturing plant.

2. Which departments have vacancies?

The openings are in Production-QMS, QC-ADL, Quality Control, Quality Management System, Regulatory Affairs, and QA-Analytical.

3. What qualifications are required?

The listed qualifications are B.Sc, M.Sc, B.Pharm, and M.Pharm.

4. How much experience is required?

The experience requirements range from 3+ years to 7 years, depending on the department.

5. What is the interview mode?

The recruitment announcement specifies a face-to-face interview.

6. How can candidates apply?

Candidates can email their updated resumes to hr.almonhc@gmail.com.

Job Summary

Category	Details
Company	Almon Healthcare Pvt. Ltd.
Vacancies	Production-QMS: 2; QC-ADL: 5; Quality Control: 8; QMS: 5; Regulatory Affairs: 4; QA-Analytical: 4
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm
Experience	3+ to 7 years, depending on the department

 

Micro Labs Ltd is inviting applications from experienced professionals for Quality Control (QC) and QC Microbiology positions.
The company is hiring for the designations of Senior Officer and Senior Executive, with opportunities in pharmaceutical quality control and microbiology.
Candidates with M.Pharm, B.Pharm, M.Sc, or M.Sc in Microbiology can apply for the relevant positions based on their qualifications and experience.
The job location is Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim, where selected candidates will work in quality control operations.

Micro Labs Ltd Recruitment: Company Overview

Micro Labs Ltd is a pharmaceutical company involved in healthcare and pharmaceutical manufacturing. The current recruitment announcement lists openings in Quality Control and QC Microbiology for candidates with relevant pharmaceutical or microbiology qualifications.

Micro Labs Ltd QC Vacancies and Job Details

1. Senior Officer / Senior Executive – Quality Control (QC)

Department: Quality Control (QC)

Designation: Senior Officer / Senior Executive

Qualification: M.Pharm / B.Pharm / M.Sc

Experience: 3–7 years

This position is intended for professionals with relevant qualifications and experience in pharmaceutical quality control.

2. Senior Officer / Executive – QC Microbiology

Department: Quality Control (Microbiology)

Designation: Senior Officer / Executive

Qualification: M.Sc in Microbiology

Experience: 1–5 years

This opportunity is suitable for microbiology professionals seeking roles in pharmaceutical quality control and microbiological operations.

Eligibility & Qualifications

Candidates must meet the qualification and experience requirements specified for the relevant position.

Educational Qualifications

• M.Pharm
• B.Pharm
• M.Sc
• M.Sc in Microbiology

Experience Requirements

• QC: 3–7 years
• QC Microbiology: 1–5 years

Candidates should select the position that matches their educational background and relevant industry experience.

Job Location and Salary

Work Location: Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim – 737132.

The recruitment announcement does not specify salary details. Compensation may depend on the selected position, relevant experience, and company policy.

How to Apply for Micro Labs Ltd Recruitment

Interested candidates can send their updated resumes to the recruitment contact provided in the announcement.

Email: santu.pal@microlabs.in

Contact Number: 6294339843

Applicants should mention the position they are applying for and include their qualifications, experience, and updated contact details in their resumes.

Documents to Keep Ready

Candidates should prepare the following documents for the recruitment process:

• Updated resume or CV
• Educational qualification certificates
• Relevant experience certificates
• Previous employment details, if applicable
• Valid contact details

Frequently Asked Questions

1. Which positions are available at Micro Labs Ltd?

The openings are for Senior Officer / Senior Executive in QC and Senior Officer / Executive in QC Microbiology.

2. What qualifications are required for QC jobs?

Candidates with M.Pharm, B.Pharm, or M.Sc qualifications are eligible for the QC position, subject to the relevant experience requirements.

3. Is M.Sc Microbiology required for QC Microbiology?

Yes. The announcement specifies M.Sc in Microbiology for the QC Microbiology position.

4. How much experience is required?

The QC position requires 3–7 years of experience, while QC Microbiology requires 1–5 years.

5. Where is the job location?

The work location is Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim – 737132.

6. How can candidates apply?

Candidates can email their updated resumes to santu.pal@microlabs.in or contact 6294339843.

Job Summary

Category	Details
Company	Micro Labs Ltd
Vacancies	Senior Officer / Senior Executive – QC; Senior Officer / Executive – QC Microbiology
Required Education	M.Pharm, B.Pharm, M.Sc, M.Sc Microbiology
Experience	QC: 3–7 years; QC Microbiology: 1–5 years

 

Lupin Walk-In Interview 2026 | Biotechnology, Biologics, Production, Engineering and GMP Compliance

Lupin is conducting a walk-in interview for experienced professionals in its Biotechnology Division and pharmaceutical manufacturing operations.
The recruitment drive covers Upstream and Downstream Production, Filling and Packaging, Visual Inspection, Engineering and Maintenance, and GMP Compliance.
Candidates with 2 to 10 years of relevant experience in biologics or biopharmaceuticals can apply for suitable opportunities.
The walk-in interview will be held on 25 October 2026 at Lemon Tree Hotel, Electronics City, Bengaluru, Karnataka.

Lupin Walk-In Interview: Company Overview

Lupin is inviting experienced candidates to explore opportunities across biotechnology, biopharmaceutical manufacturing, drug product manufacturing, engineering, and GMP compliance functions.

Lupin Recruitment 2026: Departments and Job Responsibilities

1. Biotechnology Division: Upstream and Downstream Production

The Upstream and Downstream Production function covers bioprocess manufacturing operations involving:

• Single-use bioreactors
• Fermenters
• Centrifuges
• Homogenizers
• Tangential Flow Filtration (TFF)
• Chromatography systems
• Aseptic filtration

2. Filling, Packaging and Visual Inspection

The Drug Product Manufacturing function includes filling, sterilization, packaging, and inspection operations.

Key areas include:

• Steam sterilization and filling machine operation
• Secondary packaging
• Pre-filled syringe (PFS) and vial labelling
• Blister packaging
• Check weighing
• Serialization

3. Engineering and Maintenance

The Engineering and Maintenance function covers pharmaceutical plant utilities, equipment maintenance, and technical support.

Key areas include:

• Water systems and pretreatment
• Purified Water (PW) and Water for Injection (WFI) systems
• Purified steam systems
• Calibration and alarm management
• Troubleshooting
• Instrumentation
• Heating, Ventilation and Air Conditioning (HVAC)
• Temperature mapping
• Spare parts management

4. GMP Compliance

The GMP Compliance function focuses on manufacturing compliance, quality systems, and validation activities.

Key areas include:

• Manufacturing GMP compliance
• Change control
• Deviation management
• Risk assessment
• Contamination Control Strategy (CCS)
• Cleaning validation
• Equipment qualification
• Computerized System Validation (CSV)

Eligibility and Qualifications for Lupin Recruitment

Experience Requirements

• Relevant experience: 2 to 10 years in biologics or biopharmaceuticals.

Preferred Educational Qualifications

• M.Sc. in Biotechnology or Microbiology
• M.Pharm
• B.Pharm
• B.Tech
• B.Sc. in Chemistry
• B.E. in Mechanical Engineering
• B.E. in Instrumentation Engineering
• B.E. in Electrical Engineering
• B.E. in Electronics and Telecommunication (E&TC)
• Diploma in Pharmacy
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering
• Diploma in Instrumentation Engineering
• Diploma in Electronics and Telecommunication (E&TC)
• Diploma in Chemical Engineering

Candidates should have relevant technical experience suited to the department and responsibilities they wish to pursue.

Lupin Walk-In Interview Details

Date and Time

• Date: Sunday, 25 October 2026
• Time: 9:00 AM to 5:30 PM
• Interview availability: Candidates can attend at any time during the stated interview hours.

Interview Venue

Lemon Tree Hotel, Electronics City

54B/55A, Hosur Main Road, Phase 1, Electronics City, Bengaluru – 560100, Karnataka, India.

How to Apply

Eligible candidates with 2 to 10 years of relevant experience in biologics or biopharmaceuticals can attend the walk-in interview directly at the specified venue.

Candidates should carry an updated resume and relevant educational and employment documents. The recruitment information provided does not specify an application email address or online registration link.

Documents to Carry

Candidates should prepare the following documents for the interview:

• Updated resume
• Educational certificates
• Relevant experience certificates
• Employment records and other supporting documents

Frequently Asked Questions

1. What is the experience requirement for Lupin recruitment?

Candidates should have 2 to 10 years of relevant experience in biologics or biopharmaceuticals.

2. Which qualifications are preferred?

Preferred qualifications include M.Sc. Biotechnology, M.Sc. Microbiology, M.Pharm, B.Pharm, B.Tech, B.Sc. Chemistry, relevant engineering degrees, and relevant diploma qualifications.

3. When is the Lupin walk-in interview?

The walk-in interview is scheduled for Sunday, 25 October 2026.

4. What are the interview timings?

Candidates can attend between 9:00 AM and 5:30 PM.

5. Where is the interview venue?

The interview will take place at Lemon Tree Hotel, Electronics City, Hosur Main Road, Bengaluru, Karnataka.

6. Can candidates attend at any time during the interview?

Yes. The announcement states that candidates can attend at any time throughout the scheduled interview day.

Job Summary

Category	Details
Company	Lupin
Vacancies	Biotechnology Production, Filling and Packaging, Visual Inspection, Engineering and Maintenance, GMP Compliance
Required Education	M.Sc. Biotechnology/Microbiology, M.Pharm, B.Pharm, B.Tech, B.Sc. Chemistry, relevant B.E. and Diploma qualifications
Experience	2–10 years in biologics or biopharmaceuticals

Navin Molecular Recruitment – Production Officer & Senior Officer Walk-In Interview 2026

Navin Molecular is conducting a walk-in interview on 24 October 2026 for Officer – Production and Senior Officer – Production positions at its manufacturing facility in Dewas, Madhya Pradesh. Candidates with qualifications in Chemical Engineering or Chemistry can apply, with experience requirements ranging from 0–4 years for Officer – Production and 5–6 years for Senior Officer – Production. Applicants should have hands-on experience in batch processing within chemical, pharmaceutical, API, intermediate, or specialty chemical manufacturing environments. Interested candidates should attend the interview with a hard copy of their CV or email their resumes if unable to attend in person.

Company Overview

Navin Molecular is a contract development and manufacturing organization (CDMO) providing services to pharmaceutical clients. It belongs to the Padmanabh Mafatlal Group and operates as part of Navin Fluorine International Limited’s manufacturing network. The Dewas facility supports CDMO services for pharmaceutical clients worldwide.

Job Details

Available Positions & Qualifications

1. Officer – Production

• Qualification: B.Tech, Diploma in Chemical Engineering, or M.Sc. Chemistry.

• Experience: 0–4 years.

• Suitable candidates: Applicants with relevant manufacturing or batch-processing experience in chemical, pharmaceutical, API, intermediate, or specialty chemical operations.

2. Senior Officer – Production

• Qualification: B.Tech, Diploma in Chemical Engineering, or M.Sc. Chemistry.

• Experience: 5–6 years.

• Suitable candidates: Experienced professionals with hands-on production and batch-processing expertise in chemical or pharmaceutical manufacturing.

Job Responsibilities & Technical Requirements

The recruitment announcement highlights the following responsibilities and technical expectations:

• Work in rotational shifts and participate actively in shop-floor manufacturing operations.

• Perform batch-processing activities in chemical, pharmaceutical, API, intermediate, or specialty chemical manufacturing environments.

• Work with unit operations such as distillation, crystallization, extraction, filtration, drying, and solvent recovery.

• Handle processes involving high-pressure or high-temperature reactions.

• Monitor process parameters during manufacturing operations.

• Ensure compliance with current Good Manufacturing Practices (cGMP) and safety requirements.

• Troubleshoot process deviations and support corrective actions.

• Contribute to efficient batch execution while maintaining product quality and productivity targets.

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

B.Tech in Chemical Engineering, Diploma in Chemical Engineering, or M.Sc. Chemistry.

Experience requirements depend on the position:

• Officer – Production: 0–4 years.

• Senior Officer – Production: 5–6 years.

Hands-on manufacturing experience in relevant chemical or pharmaceutical operations is an important requirement.

Walk-In Interview Details

Required Documents

– Hard copy of your updated CV.

Candidates who cannot attend the interview in person may email their CVs to the recruitment address.

How to Apply

Interested candidates can attend the walk-in interview directly at the Dewas manufacturing facility on 24 October 2026, between 10:00 AM and 2:00 PM.

Candidates unable to attend in person can email their CV to:

Email: careers.dewas@navinmolecular.com

Applicants should mention the position they are applying for — Officer – Production or Senior Officer – Production — and highlight their relevant manufacturing experience.

Job Summary

Sun Pharma Recruitment – Officer QC / Production

Sun Pharma is hiring Officer – QC / Production professionals for its API pharmaceutical operations in Madurantakam and Chengalpattu, Tamil Nadu. Candidates with 2–5 years of relevant experience in Quality Control (QC) or Production in the API pharmaceutical industry are eligible to apply. The company is seeking candidates with qualifications in Chemistry, Pharmacy, or Chemical Engineering, with preference for immediate joiners. Interested candidates can share their updated resumes directly with the recruitment contact.

Company Overview

Sun Pharmaceutical Industries is a global pharmaceutical company focused on providing quality medicines and improving patient health. This recruitment opportunity is for professionals interested in QC or Production roles within the active pharmaceutical ingredient (API) industry.

Job Details

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

• B.Sc. Chemistry

• M.Sc. Chemistry

• B.Pharm

• Diploma in Chemical Engineering

Experience Requirements

• 2–5 years of relevant experience in Quality Control or Production.

• Experience must be relevant to the API pharmaceutical industry.

• Immediate joiners are preferred.

Job Responsibilities

The recruitment announcement does not provide detailed responsibilities for the Officer – QC / Production position. Candidates should confirm the specific duties with the recruitment team.

Depending on the assigned role, relevant experience in pharmaceutical QC or API Production will be important.

Job Location

The openings are for the following locations in Tamil Nadu:

• Madurantakam

• Chengalpattu

How to Apply

Interested and eligible candidates can send their updated resumes to the recruitment email address.

• Email: seema.m1@sunpharma.com

• Suggested email subject: Application for Officer – QC / Production

Candidates should highlight their qualifications, API industry experience, QC or Production expertise, and availability to join in their applications.

Job Summary

Apitoria Pharma Recruitment – Quality Control (QC) Professionals

Apitoria Pharma Private Limited, a 100% subsidiary of Aurobindo Pharma Limited, is hiring experienced Quality Control (QC) professionals for its Active Pharmaceutical Ingredients (API) division in Visakhapatnam, Andhra Pradesh. Candidates with 3–6 years of experience and qualifications in M.Sc. Chemistry, M.Sc. Microbiology, or B.Pharmacy are invited to apply. The opportunity is suitable for professionals with knowledge of HPLC, GC, Quality Management Systems (QMS), microbiology, and pharmaceutical quality regulations. Interested candidates can submit their resumes directly to the recruitment team.

Company Overview

Apitoria Pharma Private Limited is a wholly owned subsidiary of Aurobindo Pharma Limited. The company is recruiting experienced QC professionals for its API division at its Visakhapatnam location.

Job Details

Job Role & Responsibilities

The selected candidates will support Quality Control activities in the API division.

Key responsibilities based on the recruitment announcement include:

• Perform analytical testing and related Quality Control activities.

• Work with analytical instruments and techniques, including HPLC and GC.

• Support Quality Management System (QMS) activities.

• Apply microbiological testing knowledge where relevant to assigned responsibilities.

• Maintain accurate quality documentation.

• Handle investigations related to QC activities.

• Follow current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), data integrity requirements, and applicable regulatory standards.

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

M.Sc. Chemistry, M.Sc. Microbiology, or B.Pharmacy.

Experience Requirements

• 3–6 years of relevant experience in Quality Control.

• Experience in analytical testing, documentation, and investigation handling.

• Familiarity with pharmaceutical quality systems and regulatory requirements.

Required Skills

Applicants should have good knowledge of:

• High-Performance Liquid Chromatography (HPLC).

• Gas Chromatography (GC).

• Quality Management Systems (QMS).

• Microbiology.

• Current Good Manufacturing Practices (cGMP).

• Good Laboratory Practices (GLP).

• Data integrity and regulatory requirements.

• Analytical testing and quality documentation.

• Investigation handling.

Job Location

The positions are for the API division in Visakhapatnam, Andhra Pradesh, India.

How to Apply

Interested candidates with relevant Quality Control experience can send their updated resumes directly to the recruitment contact.

• Email: arunkumar.komshetpally@apitoria.com

• Suggested email subject: Application for QC Position – API Division, Visakhapatnam

Candidates should highlight their experience with HPLC, GC, QMS, analytical testing, documentation, and investigation handling in their resumes.

Job Summary

Fortrea Recruitment – Site Navigator I

Fortrea is hiring a Site Navigator I for its clinical research operations in India. This full-time opportunity is available to candidates based in Bangalore, Hyderabad, Pune, Mumbai, and other locations across India through a remote working arrangement. The role focuses on clinical trial site start-up, feasibility assessments, regulatory submissions, essential document management, and site activation. Candidates with a relevant degree or equivalent experience, knowledge of ICH-GCP guidelines, and experience in clinical research or related fields can apply.

Company Overview

Fortrea is a global clinical research services company supporting pharmaceutical and biotechnology organizations in clinical development. The Site Navigator I role helps coordinate investigative site activities, maintain regulatory compliance, and support the timely initiation and management of clinical studies.

Job Details

Job Role & Responsibilities

The Site Navigator I will coordinate clinical trial site activities from feasibility and initial outreach through site activation and, when required, study closeout. The role serves as a primary point of contact for investigative sites and supports collaboration between sponsors, CRO teams, and site staff.

Key responsibilities include:

• Coordinate site-level tasks for efficient site activation in compliance with ICH-GCP guidelines, local regulations, SOPs, and project requirements.

• Identify potential research sites and assess their capabilities, resources, and suitability for clinical studies.

• Conduct initial site outreach, obtain confidentiality agreements, and collect feasibility surveys.

• Perform remote pre-study visits, prepare visit documentation, and complete trip reports.

• Support customization and translation of informed consent forms (ICFs) and patient-facing materials.

• Collect, track, and quality-check essential documents required for site selection, regulatory submissions, and site activation.

• Monitor site regulatory compliance, including applicable ethics committee renewals, principal investigator changes, and document expirations.

• Participate in study team meetings and develop action plans for site-level risks, delays, and performance issues.

• Support Clinical Research Associate (CRA) teams in preparing for Site Initiation Visits (SIVs).

• Coordinate clinical study supplies, access requirements, and documentation with vendors and study teams.

• Prepare submissions to and liaise with Institutional Review Boards (IRBs), Independent Ethics Committees (IECs), third bodies where applicable, and regulatory authorities.

• Collaborate with Global Regulatory Submissions Leads on regulatory submissions.

• Conduct initial site contract and budget negotiations, including amendments where applicable.

• Maintain accurate essential documents and keep the Trial Master File (TMF) audit-ready.

• Track site start-up progress and ensure that milestones and deadlines are met.

• Serve as the primary contact for investigative sites and support timely delivery within the study scope and budget.

• Perform Case Report Form (CRF) reviews and validate clinical data against source documentation, as applicable.

• Support monitoring of protocol deviations, Serious Adverse Event (SAE) reporting, and other study activities as assigned.

Eligibility & Qualifications

Candidates should meet one of the qualification pathways specified by Fortrea:

• University or college degree, preferably in Life Sciences.

• Certification in a related allied health profession from an accredited institution, such as nursing, medical technology, or laboratory technology.

• Alternatively, 2–3 years of work experience in clinical research, including working knowledge of ICH-GCP guidelines and regulatory authority and IRB/IEC regulations.

• Fortrea may consider relevant equivalent experience instead of the stated educational requirements.

• Candidates with a high school diploma or equivalent and at least 5 years of clinical research experience, including strong knowledge of ICH-GCP and regulatory and IRB/IEC requirements, may also be considered under the alternative pathway.

Candidates must be fluent in the relevant local official language and English, both written and spoken.

Experience Requirements

Fortrea identifies the following experience and knowledge as important for this role:

• At least one year of experience in a related field, such as medical, clinical, pharmaceutical, or laboratory research, data analysis, data management, or technical writing.

• One year of clinical research experience is preferred.

• Basic knowledge of ICH-GCP, regulatory authority requirements, IRB/IEC regulations, and applicable clinical research guidelines.

• Familiarity with investigator site start-up documents and contract and budget negotiations.

• Understanding of clinical research protocols and study requirements.

• Experience interacting with operational project teams and investigative sites is preferred.

Required Skills & Competencies

Applicants should demonstrate:

• Strong written and verbal communication skills.

• Ability to coordinate with site staff, CRO personnel, sponsors, and regulatory authorities.

• Effective organization and time management.

• Ability to manage multiple tasks, competing priorities, and deadlines.

• Understanding of clinical trial regulations and compliance requirements.

• Problem-solving skills to identify and resolve site start-up issues.

• Ability to support site contract and budget negotiations.

• Attention to detail in regulatory documentation and Trial Master File maintenance.

Work Location & Environment

The position is remote-based in India, with possible office presence depending on the candidate’s location. Travel requirements are limited to training, according to the job description.

Listed locations include:

• Bangalore, Karnataka

• Hyderabad, Telangana

• Pune, Maharashtra

• Mumbai, Maharashtra

• Remote India

How to Apply

Interested candidates can review the complete job description and apply through Fortrea’s official careers portal.

Apply for Site Navigator I at Fortrea

Applicants should highlight relevant clinical research experience, ICH-GCP knowledge, regulatory documentation skills, site start-up experience, and familiarity with clinical trial workflows in their resumes.

Job Summary

Nova IVF Fertility Recruitment 2026: Multiple Job Openings

Nova IVF Fertility is inviting applications for multiple positions at its Hajipur, Bihar centre. The recruitment drive includes opportunities for Staff Nurses, Pharmacists, Customer Care Executives, Andro Technicians and NFC Executives.
Candidates with qualifications such as GNM, B.Sc Nursing, D.Pharm, B.Pharm, Diploma, B.Sc, M.Sc in Microbiology, M.Sc Life Sciences and other graduate qualifications can apply for suitable roles.
Applicants should have 1–5 years of experience, depending on the position, and nursing or pharmacy candidates must hold the required State Nursing Council or Pharmacy Council registration.
Interested candidates can send their updated CVs to the recruitment email address provided below.

H2: Nova IVF Fertility Recruitment 2026

Nova IVF Fertility has announced openings across clinical support, pharmacy, customer care and laboratory-related functions at its Hajipur centre. Candidates with the required educational qualifications and relevant work experience can apply for the positions listed in the recruitment notice.

H2: Nova IVF Fertility Vacancy Details

Position	Qualification	Experience
Staff Nurse	GNM / B.Sc Nursing	1–3 years
Pharmacist	D.Pharma / B.Pharma	1–5 years
Executive – Customer Care	Diploma / Any Graduate	1–3 years
Andro Technician	B.Sc / M.Sc in Microbiology / M.Sc Life Sciences	2–4 years
Executive – NFC	Any Graduate	1–3 years

H2: Job Role and Responsibilities

H3: Staff Nurse

The Staff Nurse position is suitable for candidates with a GNM or B.Sc Nursing qualification and 1–3 years of experience. Applicants must have the required nursing council registration.

H3: Pharmacist

Candidates with a Diploma in Pharmacy or Bachelor of Pharmacy and 1–5 years of experience can apply for the Pharmacist position. State Pharmacy Council registration is mandatory.

H3: Executive – Customer Care

Candidates with a diploma or any graduate qualification and 1–3 years of experience are eligible to apply for the Customer Care Executive position.

H3: Andro Technician

The Andro Technician role is open to candidates with a B.Sc or M.Sc in Microbiology or an M.Sc in Life Sciences. Applicants should have 2–4 years of relevant experience.

H3: Executive – NFC

Candidates with any graduate qualification and 1–3 years of experience can apply for the NFC Executive position.

H2: Eligibility and Qualifications

Applicants should meet the educational and experience requirements specified for their preferred role.

Eligible qualifications include:

• GNM
• B.Sc Nursing
• D.Pharm
• B.Pharm
• Diploma
• Any Graduate
• B.Sc in Microbiology
• M.Sc in Microbiology
• M.Sc Life Sciences

Important requirement: State Nursing Council registration is mandatory for nursing candidates, and State Pharmacy Council registration is mandatory for pharmacy candidates.

H2: Location and Experience

Job Location: Nova IVF Fertility Centre, Hajipur, Bihar.

Experience requirements vary according to the position:

• Staff Nurse: 1–3 years
• Pharmacist: 1–5 years
• Executive – Customer Care: 1–3 years
• Andro Technician: 2–4 years
• Executive – NFC: 1–3 years

H2: How to Apply

Interested and eligible candidates should follow these steps:

1. Prepare an updated CV with accurate educational qualifications and work experience.
2. Mention the position you are applying for in your email.
3. Send your CV to ipsa.mohanty@novaivffertility.com.
4. For further information, visit the official website: www.novaivffertility.com.

Candidates applying for Staff Nurse and Pharmacist positions should ensure that they meet the applicable registration requirements.

H2: Frequently Asked Questions

H3: 1. Which positions are available at Nova IVF Fertility?

The advertised openings include Staff Nurse, Pharmacist, Executive – Customer Care, Andro Technician and Executive – NFC.

H3: 2. Can freshers apply for these positions?

The advertisement specifies experience requirements ranging from 1–5 years, depending on the position. Freshers are not explicitly listed as eligible.

H3: 3. What qualifications are required for the Pharmacist position?

Candidates need a D.Pharm or B.Pharm qualification and 1–5 years of experience. State Pharmacy Council registration is mandatory.

H3: 4. What is the qualification for the Andro Technician role?

Candidates need a B.Sc or M.Sc in Microbiology or an M.Sc in Life Sciences, along with 2–4 years of experience.

H3: 5. How can candidates apply?

Candidates can email their updated CV to ipsa.mohanty@novaivffertility.com.

H3: 6. Where is the recruitment location?

The openings are for the Nova IVF Fertility centre in Hajipur, Bihar.

H2: Nova IVF Fertility Recruitment Summary

Category	Details
Company	Nova IVF Fertility
Vacancies	Staff Nurse, Pharmacist, Executive – Customer Care, Andro Technician, Executive – NFC
Required Education	GNM, B.Sc Nursing, D.Pharm, B.Pharm, Diploma, Any Graduate, B.Sc / M.Sc Microbiology, M.Sc Life Sciences
Experience	1–5 years, depending on the position