Author: Sudheer vanguri

Acme Group is conducting a Walk-In Drive for pharma professionals at its sterile and OSD formulation manufacturing sites in Baddi and Nalagarh, Himachal Pradesh.
The recruitment covers Engineering, Quality Assurance, Production, Quality Control, QC Microbiology and Packing departments.
Multiple positions are available for Staff, Technician and Operator levels with relevant pharmaceutical manufacturing experience.
Eligible candidates can attend the walk-in interview with their updated CV, ID proof, passport-size photograph and salary supporting documents.

Acme Group Walk-In Interview

Acme Group is a leading contract manufacturing group for Oral Solid Dosage and Sterile products. The company is recruiting experienced professionals for its manufacturing operations.

Engineering (Sterile) – Acme Group

Key Areas / Sub Department: Process Equipment, Vial/Ampoule Filling & Sealing, Ophthalmic Filling, PPS/Cartridge, Isolator, Compounding, Autoclave, Depyrogenation Tunnel, Lyophilizer, Vial Washing, Instrumentation, Engineering, CMS, HVAC, BMS, EMS, Utilities, Boiler, Chiller, Electrical & Water Systems, WFI, Pure Steam, Vacuum Compressors, Multicolumn Distillation and Ozone Generator.

Staff – AM / Executive / Officer

Qualification: M.Tech / B.Tech
Experience: 2–12 Years

Technician – Sr. Technician / Technician

Qualification: Diploma / ITI
Experience: 4–12 Years

Quality Assurance (Sterile) – Acme Group

Key Areas / Sub Department: IPQA, Manufacturing & Packing, Documentation & Audit Compliance, PV/CV, Media Fill, Aseptic Interventions, Sterility Assurance, Lyophilization Process, EM Monitoring, Smoke Studies, Microbial Compliance, Equipment/Utility Qualification, Investigation, RCA/Deviations/Complaints, QRM, Training, APQR and AQA.

Staff – AM / Executive / Officer

Qualification: B.Pharm / M.Sc. / M.Pharm
Experience: 2–12 Years

Production (Sterile) – Acme Group

Key Areas / Sub Department: Aseptic Area, Autoclave/TS Area, Compounding & Filling, Lyophilization, Isolator & Integrity Testing, Production QMS, Training & eDCS, Media Fill, Process Validation, BMR Review & Documentation, ERP, DWP Applications.

Staff – Sr. Executive / Executive / Officer

Qualification: B.Pharm / M.Pharm
Experience: 2–8 Years

Operator – Sr. Operator / Operator

Qualification: ITI / Diploma
Experience: 2–10 Years

Quality Control (OSD and Sterile) – Acme Group

Key Areas / Sub Department: HPLC, UPLC, GC, UV, FTIR, KF, TOC, Dissolution, RM/PM & IP/FP Testing, Stability, OOS/OOT & Data Integrity, Instrumentation, Calibration, Qualification, Validation, PM & Troubleshooting.

Staff – AM / Executive / Officer

Qualification: B.Pharm / M.Sc. / M.Pharm
Experience: 2–12 Years

QC Microbiology (OSD and Sterile) – Acme Group

Key Areas / Sub Department: EM, Water Testing, Sterility, BET/LAL, Bioburden, Media Fill, GPT, MLT, Microbial ID, Microbial Compliance & Environmental/Facility Monitoring.

Staff – AM / Executive / Officer

Qualification: M.Sc. Microbiology
Experience: 2–12 Years

Quality Assurance (OSD) – Acme Group

Key Areas / Sub Department: IPQA – OSD Manufacturing & Packing, Documentation, Audit Compliance, Validation, Vendor Qualification, Equipment/Utility Qualification, Investigations, RCA, Deviations, Complaints, QRM, Training and AQA.

Staff – AM / Executive / Officer

Qualification: B.Pharm / M.Sc. / M.Pharm
Experience: 2–12 Years

Production (OSD) – Acme Group

Key Areas / Sub Department: Granulation, Compression, Coating, Capsule Filling, Dispensing, Checkweigher, Imprinting, Inspection, TDS, Production QMS and Training.

Staff – Executive / Officer

Qualification: B.Pharm / M.Pharm
Experience: 2–8 Years

Operator – Sr. Operator / Operator

Qualification: ITI / Diploma
Experience: 2–10 Years

Packing (OSD) – Acme Group

Key Areas / Sub Department: Primary Packing, Secondary Packing, Blister (Elmach 2000, 2500, 3015), Strip, Bottle Filling & Capping, Autocomart, BQS, Bulk Line, Labelling and Serialization Machines.

Staff – Executive / Officer

Qualification: B.Sc. / B.Pharm
Experience: 2–8 Years

Operator – Sr. Operator / Operator

Qualification: ITI / Diploma
Experience: 2–10 Years

Engineering (OSD) – Acme Group

Key Areas / Sub Department: Process Equipment (RMG, FBD, Blender, Compression, Coating, Capsule, Packing & Serialization), Engineering QMS, HVAC, BMS/EMS, Utilities, Electrical & Water Systems.

Staff – Executive / Officer

Qualification: M.Tech / B.Tech
Experience: 2–8 Years

Technician – Sr. Technician / Technician

Qualification: Diploma / ITI
Experience: 2–12 Years

Eligibility & Qualifications

Eligible qualifications mentioned for the available positions include:

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

Candidates should possess the qualification and relevant API/pharmaceutical manufacturing experience specified for the position.

Experience Requirements

The required experience varies by position and department:

• Staff Positions: 2–12 Years
• Technician Positions: 2–12 Years
• Operator Positions: 2–10 Years

Candidates must have relevant experience corresponding to the advertised department and role.

Walk-In Interview Details

Date: 27 September 2026, Sunday
Time: 09:30 AM to 04:00 PM

Venue – Acme Group

The Legend Sarovar Portico
Vill. Malpur, Tehsil Baddi
Distt. Solan, Himachal Pradesh – 173205

Documents Required

Interested and eligible candidates are advised to appear for the walk-in interview along with:

• Updated CV
• ID proof
• Passport-size photograph
• Salary supporting documents

How to Apply

Candidates who meet the eligibility criteria can attend the walk-in interview at the above venue.

For queries, contact:

Phone: 8580412182 / 7018194189

Candidates can also send their CV to:

Email: recruitment@immacule.in
Email: career@acmeformulation.com

Website: www.acmegenerics.in

Job Summary

Bharat Biotech is looking for talented and motivated professionals to join its team and contribute to the development of life-saving vaccines.
The current openings are available across Production, MSAT and IPQA functions.
Candidates with relevant pharmaceutical, biotechnology and life sciences qualifications can apply for these positions.
Vaccine manufacturing experience is preferred, with experience requirements ranging from 3 to 10 years depending on the role.

Bharat Biotech – Production, MSAT & IPQA Jobs

Production Department – Bharat Biotech

Experience: 3–5 Years

Education: M.Sc. / M.Tech. / M.Pharm.

Job Description

• Vaccine formulation development and physicochemical characterization.
• Antigen adsorption at GMP scale, including bulk and formulations, liquid and lyophilised.
• Handle basic GMP documentation such as SOPs, protocols and reports.
• Operate GLP equipment including viscometers, particle size analyser, lyophiliser, centrifuges, homogenisers, pH and conductivity meters, etc.

MSAT Department – Bharat Biotech

Experience: 3–6 Years

Education: M.Sc. / M.Tech. / M.Pharm. in relevant Life Sciences or Biotechnology disciplines.

Job Description

• Routine mammalian adherent cell culture under aseptic conditions.
• Monitor cell morphology, viability and growth.
• Work with large-scale systems including T75, T175, roller bottles, cell stacks and cell factories.
• Apply cGMP and aseptic techniques, filtration techniques, and preparation of cell and virus banks.

IPQA Department – Bharat Biotech

Experience: 8–10 Years

Education: M.Pharm. / M.Sc. in Biotechnology, Microbiology or Life Sciences.

Job Description

• Ensure GMP and regulatory compliance for vaccine manufacturing and quality.
• Review and approve batch records, deviations, CAPA, change controls and investigations related to process.
• Conduct line clearances, process validations and cleaning validations.
• Support quality risk management and continual improvement initiatives.
• Ensure proper documentation and adherence to SOPs.

Eligibility & Qualifications

Production – Bharat Biotech

M.Sc. | M.Tech. | M.Pharm.

Candidates with relevant experience in vaccine formulation development, physicochemical characterization, GMP documentation and related manufacturing activities can apply.

MSAT – Bharat Biotech

M.Sc. | M.Tech. | M.Pharm.

The qualification should be in relevant Life Sciences or Biotechnology disciplines.

IPQA – Bharat Biotech

M.Pharm. | M.Sc.

Relevant specialisations include:

Biotechnology | Microbiology | Life Sciences

Experience Requirements

• Production: 3–5 Years
• MSAT: 3–6 Years
• IPQA: 8–10 Years

Preferred Experience

Vaccine experience is preferred for the available positions.

How to Apply

Interested candidates can apply by sending their CV to:

Email: samiksha6596@bharatbiotech.com

Candidates should mention the relevant position in the email subject line:

Production / MSAT / IPQA

Job Summary

Provis is hiring experienced professionals for a Quality Control – Analytical position.
The opening is for candidates with an M.Sc. in Biotechnology and relevant experience in analytical quality control.
Candidates with 2–6 years of experience can apply, with biotechnology experience preferred.
The position is based in Kukatpally, Hyderabad, and willingness to work in shifts is required.

Provis Biolabs – QC Analytical

Quality Control – Analytical | Provis Biolabs

Provis Biolabs is looking for an experienced professional to join its Quality Control Department as a QC – Analytical professional.

Experience: 2–6 Years
Qualification: M.Sc. Biotechnology
Preference: Biotechnology experience preferred
Location: Kukatpally, Hyderabad
Work Requirement: Willingness to work in shifts is required.

Key Responsibilities – QC Analytical

• Perform physical, chemical and performance-based testing of raw materials, intermediates, finished products, packaging materials, stability and in-process samples using instruments such as HPLC, UV-Vis spectrophotometers and others.
• Receive samples, allocate AR numbers, perform testing, document and report analytical results.
• Withdraw and aliquot batch release and stability samples for analysis.
• Prepare, revise and maintain SOPs, STPs, specifications, stability protocols, reports and worksheets.
• Compile and interpret test data to prepare comprehensive analytical reports.
• Report and document any OOS, OOT or deviations.
• Plan and execute analytical method validations.
• Perform BET testing for product samples and water samples.
• Verify SOPs, STPs and analytical reports to ensure compliance and accuracy.
• Ensure all testing methods are aligned with ICH, USP and EP and comply with regulatory and GMP requirements, including FDA requirements.
• Prepare various protocols and reports related to product testing.
• Conduct inspections of finished products, in-process samples and raw materials to ensure they meet defined specifications.

Eligibility & Qualifications

M.Sc. Biotechnology

Candidates with relevant biotechnology experience are preferred for this Quality Control – Analytical position.

Experience Required

2–6 Years

Relevant experience in Quality Control, analytical testing, laboratory testing, analytical methods, documentation and pharmaceutical/biological product testing would be applicable to the role.

Department & Job Location

Department: Quality Control
Position: QC – Analytical
Location: Kukatpally, Hyderabad
Industry: Biologics / Pharmaceutical

How to Apply

Interested candidates can share their updated CV with:

Email: careers@provisbiolabs.com

Candidates should ensure that their resume clearly mentions their qualification, relevant QC experience and analytical laboratory skills.

Note: Provis Biolabs states that it does not charge anything for recruitment.

Job Summary

Edara Research Foundation is hiring professionals for multiple research and laboratory positions.
The openings cover Ecotoxicology, Quality Assurance, Clinical Pathology, Histopathology and Genetic Toxicology.
Candidates with qualifications ranging from DMLT and Bachelor’s degrees to postgraduate qualifications in Biological Sciences can apply.
Relevant experience is required according to the position, with opportunities available from 0 to 8 years of experience.

Edara Research Foundation – Open Positions

Edara Research Foundation is looking for candidates to join its research team and contribute to meaningful scientific research. The available positions include Ecotoxicology – Study Director, QA Personnel, Clinical Pathology Technician, Histopathology Technician and Genetic Toxicology – Study Director.

Ecotoxicology – Study Director | Edara Research Foundation

Experience: 4–8 Years

Minimum Qualification: Postgraduate in Biological Sciences

The Ecotoxicology Study Director position is suitable for candidates with relevant postgraduate qualifications in Biological Sciences and experience in the relevant research area.

QA Personnel | Edara Research Foundation

Experience: 0–2 Years

Minimum Qualification: Postgraduate in Biological Sciences

Candidates with a postgraduate qualification in Biological Sciences and relevant experience can apply for the Quality Assurance position.

Clinical Pathology Technician | Edara Research Foundation

Experience: 0–2 Years

Minimum Qualification: Bachelor’s Degree

Candidates with a Bachelor’s degree and relevant clinical pathology or laboratory background can apply.

Histopathology Technician | Edara Research Foundation

Experience: 0–1 Years

Minimum Qualification: DMLT

Candidates with a Diploma in Medical Laboratory Technology (DMLT) and relevant laboratory knowledge can apply.

Genetic Toxicology – Study Director | Edara Research Foundation

Experience: 2–4 Years

Minimum Qualification: Postgraduate in Biological Sciences

Candidates with a postgraduate qualification in Biological Sciences and relevant experience in genetic toxicology or related research areas can apply.

Eligibility & Qualifications

The following qualifications are mentioned for the respective positions:

Postgraduate in Biological Sciences | Bachelor’s Degree | DMLT

Ecotoxicology – Study Director

Postgraduate in Biological Sciences

QA Personnel

Postgraduate in Biological Sciences

Clinical Pathology Technician

Bachelor’s Degree

Histopathology Technician

DMLT

Genetic Toxicology – Study Director

Postgraduate in Biological Sciences

Experience Requirements

• Ecotoxicology – Study Director: 4–8 Years
• QA Personnel: 0–2 Years
• Clinical Pathology Technician: 0–2 Years
• Histopathology Technician: 0–1 Years
• Genetic Toxicology – Study Director: 2–4 Years

Important Note

Only relevant applications will be considered based on the qualifications and experience mentioned above.

How to Apply

Interested candidates should send their updated resume to the following email addresses:

Email: hr@edararesearch.com
Email: bd@edararesearch.com

Candidates are advised to mention the relevant position clearly when submitting their application.

Job Summary

Neuland Laboratories Limited is conducting a Walk-In Interview for multiple positions across Production, Safety, Plant Engineering, Quality Control, Quality Assurance and Stores/Warehouse departments. The openings include opportunities for Freshers, Chemists, Officers, Executives and Assistant Managers. Candidates with qualifications including B.Sc Chemistry, M.Sc Chemistry, B.Tech Chemical Engineering and B.Tech Mechanical can apply for the respective positions.

Neuland Laboratories Limited – Walk-In Interview

Walk-In Interview Details

Interview / Work Location: Neuland Laboratories Limited
Unit-1, Bonthapally, Hyderabad, Telangana

Date: 9th & 10th October 2026
Time: 10:00 AM to 16:00

Production Department – Neuland Laboratories

Fresher / Chemist – Intermediates / Clean Rooms

Designation: Fresher / Chemist
Role: Intermediates / Clean Rooms
Experience: 0 – 4 Years
Qualification: B.Sc Chemistry / M.Sc Chemistry / B.Tech (Chemical Engineering)

Candidates with relevant Chemistry or Chemical Engineering qualifications can apply for the Production position.

Chemist / Executive – Peptide

Designation: Chemist / Executive
Role: Peptide
Experience: 3 – 10 Years
Qualification: B.Sc Chemistry / M.Sc Chemistry / B.Tech (Chemical Engineering)

Candidates with relevant experience in peptide manufacturing can apply.

Safety Department – Neuland Laboratories

Assistant Manager – Process Safety

Designation: Assistant Manager
Role: Process Safety
Experience: 10 – 11 Years
Qualification: B.Tech (Chemical)

Candidates with relevant process safety experience and a B.Tech Chemical qualification can apply.

Plant Engineering Department – Neuland Laboratories

Officer / Executive – Maintenance

Designation: Officer / Executive
Role: Maintenance
Experience: 6 – 10 Years
Qualification: B.Tech (Mechanical)

Candidates with relevant plant maintenance experience can apply.

Executive – Civil

Designation: Executive
Role: Civil
Experience: 8 – 10 Years
Qualification: B.Tech (Mechanical)

The recruitment notification lists B.Tech (Mechanical) as the qualification for this position.

Quality Control Department – Neuland Laboratories

Officer – HPLC

Designation: Officer
Role: HPLC
Experience: 5 – 7 Years
Qualification: M.Sc (Chemistry)

Candidates with relevant HPLC and Quality Control experience can apply.

Quality Assurance Department – Neuland Laboratories

Officer / Executive – IPQA / AQA

Designation: Officer / Executive
Role: IPQA / AQA
Experience: 5 – 10 Years
Qualification: M.Sc (Chemistry)

Candidates with relevant experience in IPQA / AQA can apply.

Stores / Warehouse Department – Neuland Laboratories

Officer – QMS Activities / Dispensing

Designation: Officer
Role: QMS Activities / Dispensing
Experience: 5 – 7 Years
Qualification: B.Sc (Chemistry)

Candidates with relevant experience in QMS activities and dispensing can apply.

Eligibility & Qualifications

Candidates with the following qualifications are eligible for the respective positions:

B.Sc Chemistry | M.Sc Chemistry | B.Tech Chemical Engineering | B.Tech Chemical | B.Tech Mechanical

Production – Intermediates / Clean Rooms

B.Sc Chemistry | M.Sc Chemistry | B.Tech (Chemical Engineering)

Production – Peptide

B.Sc Chemistry | M.Sc Chemistry | B.Tech (Chemical Engineering)

Safety – Process Safety

B.Tech (Chemical)

Plant Engineering – Maintenance

B.Tech (Mechanical)

Plant Engineering – Civil

B.Tech (Mechanical)

Quality Control – HPLC

M.Sc (Chemistry)

Quality Assurance – IPQA / AQA

M.Sc (Chemistry)

Stores / Warehouse – QMS Activities / Dispensing

B.Sc (Chemistry)

Experience Required

• Production – Intermediates / Clean Rooms: 0 – 4 Years
• Production – Peptide: 3 – 10 Years
• Safety – Process Safety: 10 – 11 Years
• Plant Engineering – Maintenance: 6 – 10 Years
• Plant Engineering – Civil: 8 – 10 Years
• Quality Control – HPLC: 5 – 7 Years
• Quality Assurance – IPQA / AQA: 5 – 10 Years
• Stores / Warehouse – QMS Activities / Dispensing: 5 – 7 Years

Key Functional Areas

Production

• Intermediates
• Clean Rooms
• Peptide manufacturing

Safety

• Process Safety

Plant Engineering

• Maintenance
• Civil

Quality Control

• HPLC

Quality Assurance

• IPQA
• AQA

Stores / Warehouse

• QMS Activities
• Dispensing

Important Note

The recruitment notification states that the mentioned qualification and API experience are mandatory.

Candidates attending the interview are requested to carry:

• Latest updated CV
• Last 3 months’ payslips
• Latest increment letter

How to Apply

Interested candidates can attend the Neuland Laboratories Walk-In Interview on 9th and 10th October 2026, between 10:00 AM and 16:00.

Walk-In Venue

Neuland Laboratories Limited
Unit-1, Bonthapally, Hyderabad, Telangana

Candidates should carry their updated CV, last 3 months’ payslips and latest increment letter to the interview.

CV Submission

Candidates can also reach out to:

Email: adviyani@neulandlabs.com

Job Summary

Amneal Pharmaceuticals is conducting a Walk-In Drive at its Pipan Plant, Ahmedabad for candidates with relevant experience in an injectable regulated pharmaceutical plant.
The openings are available across Manufacturing, Quality Assurance and Quality Control departments.
Positions include Assistant, Associate, Officer and Executive roles with experience requirements ranging from 1 to 6 years.
Candidates with ITI, Diploma, B.Sc., B.Pharm., M.Pharm. and M.Sc. qualifications can apply for the respective positions.

Amneal Pharmaceuticals – Walk-In Drive

Walk-In Interview Details

Date: 27th September 2026, Sunday
Time: 9:00 AM to 2:00 PM

Venue

Amneal Pharmaceuticals Pvt. Ltd.
Plot No. 161/1, Sanand Bavla Highway Road,
Village: Pipan, Sanand, Ahmedabad, Gujarat – 382110

Manufacturing Department – Amneal Pharmaceuticals

Assistant / Associate – Manufacturing

Department: Manufacturing (Production)
Location: Ahmedabad
Qualification: ITI / Diploma / D.Pharm. / B.Sc.
Experience: 1 to 6 Years

Required Skills

• Hands-on experience in complex manufacturing equipment such as Emulsion and Suspension.
• Experience in Vial & Bag Filling machines, including SHINVA Bag Filling and PLUMAT Line.
• Experience in Emulsion / Suspension.
• Experience in Bag Line.
• Experience in Inhalation Line.
• Experience with PFS.
• Experience with LYO.
• Experience with Cartridges.
• Experience with Filling Machine with Isolator.

Candidates should have relevant experience in an injectable regulated pharmaceutical plant.

Quality Assurance Department – Environmental Monitoring

Officer / Executive – QA Environmental Monitoring

Department: QA – EM (Environmental Monitoring)
Location: Ahmedabad
Qualification: B.Sc. Microbiology / M.Sc. Microbiology
Experience: 1 to 5 Years

Required Skills

• Experience in Environmental Monitoring.
• Experience in non-viable particle monitoring of sterile / aseptic manufacturing plants.

Quality Assurance Department – IPQA & Validation

Officer / Executive – QA IPQA & Validation

Department: QA – IPQA & Validation
Location: Ahmedabad
Qualification: B.Pharm. / M.Pharm. / M.Sc.
Experience: 2 to 6 Years

Required Skills

• Hands-on experience in line clearance and validation activities for manufacturing and packing areas.
• Experience in BMR and BPR review.
• Experience in shop floor compliance.
• Experience in visual inspection qualification.
• Candidates having media fill exposure will be preferred.

Quality Control Department – QCC

Officer / Executive – Quality Control

Department: Quality Control (QCC)
Location: Ahmedabad
Qualification: B.Pharm. / M.Pharm. / M.Sc.
Experience: 2 to 6 Years

Required Skills

• Hands-on experience in raw material testing.
• Experience in in-process product testing (IPPT).
• Experience in finished product (FP) testing.
• Experience with analytical instruments such as:

  • ICP-MS
  • ICP-OES
  • HPLC
  • UV
  • GC

Eligibility & Qualifications

Candidates with the following qualifications are eligible for the respective positions:

ITI | Diploma | D.Pharm. | B.Sc. | B.Pharm. | M.Pharm. | M.Sc.

Manufacturing – Production

ITI | Diploma | D.Pharm. | B.Sc.

QA – Environmental Monitoring

B.Sc. Microbiology | M.Sc. Microbiology

QA – IPQA & Validation

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

Quality Control – QCC

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

Experience Required

• Manufacturing – Production: 1 to 6 Years
• QA – Environmental Monitoring: 1 to 5 Years
• QA – IPQA & Validation: 2 to 6 Years
• Quality Control – QCC: 2 to 6 Years

Key Experience Areas

Manufacturing – Injectable Production

Relevant experience in:

• Emulsion
• Suspension
• Vial Filling
• Bag Filling
• PFS
• Inhalation Line
• LYO
• Cartridges
• Filling Machine with Isolator

Quality Assurance – Environmental Monitoring

Relevant experience in:

• Environmental Monitoring
• Non-Viable Particle Monitoring
• Sterile Manufacturing
• Aseptic Manufacturing

Quality Assurance – IPQA & Validation

Relevant experience in:

• Line Clearance
• Validation Activities
• Manufacturing and Packing Areas
• BMR / BPR Review
• Shop Floor Compliance
• Visual Inspection Qualification
• Media Fill

Quality Control – QCC

Relevant experience in:

• Raw Material Testing
• In-Process Product Testing (IPPT)
• Finished Product Testing (FP)
• ICP-MS
• ICP-OES
• HPLC
• UV
• GC

Pharmaceutical Industry Experience

Candidates must have relevant experience in an injectable regulated pharmaceutical plant as specified in the recruitment notification.

How to Apply

Interested candidates can attend the Amneal Pharmaceuticals Walk-In Drive on 27th September 2026, between 9:00 AM and 2:00 PM.

Candidates who are unable to attend the interview can share their CV through email.

CV Submission

Email: ajaykumar.pandey@amneal.com
Email: Anurag.saroj@amneal.com

Candidates should use the following subject line when applying:

Application for INJ Mfg/ QA/ EM/ QCC

Candidates can also scan the QR code in the recruitment notification to apply online.

Job Location

Amneal Pharmaceuticals – Pipan Plant

Plot No. 161/1, Sanand Bavla Highway Road, Village: Pipan, Sanand, Ahmedabad, Gujarat – 382110

Important Note

Amneal states that it provides equal job opportunities and does not charge applicants for employment or authorize any agency to collect fees for recruitment.

Job Summary

Aculife Healthcare Private Limited is conducting a Walk-In Interview for the position of Production Chemist in its Production Department. The opportunity is open to freshers as well as candidates with up to 5 years of experience. Candidates with B.Sc, M.Sc, B.Pharm or M.Pharm qualifications can apply. The role involves sterile infusion manufacturing, including Parenteral, FFS, BFS and Bottle Pack systems, with a focus on GMP, safety and quality requirements.

Aculife Healthcare Private Limited – Production Chemist

Walk-In Interview Details

Position: Production Chemist
Department: Production
Experience: 0 to 5 Years
Qualification: B.Sc. / M.Sc. / B.Pharm. / M.Pharm.

Date: 03-10-2026, Saturday
Time: 09:00 AM to 02:00 PM

Venue

Aculife Healthcare Private Limited
Near Railway Crossing (Sanand – Viramgam Highway)
Village: Sachana, Taluka – Viramgam
District: Ahmedabad – 382150

Production Department – Aculife Healthcare

Production Chemist

The Production Chemist will be responsible for the manufacturing of sterile infusion products in Parenteral, FFS, BFS and Bottle Pack systems, while ensuring compliance with GMP, safety and quality requirements.

Key Responsibilities

• Execute sterile infusion manufacturing as per BMR / SOP.
• Operate Parenteral filling machines, including FFS / BFS / Blow Fill Seal / Bottle Pack systems.
• Monitor production parameters and maintain batch records.
• Ensure line clearance before batch start-up.

Required Experience

Production Chemist – Aculife Healthcare

Experience: 0 to 5 Years

The recruitment is open to fresh graduates as well as candidates with relevant experience.

Relevant Manufacturing Experience

Experience in the following areas is relevant:

• Sterile Manufacturing
• Injectable Manufacturing
• Infusion Manufacturing
• Plastic Parenteral systems
• FFS
• BFS
• Bottle Pack systems

Eligibility & Qualifications

Candidates with the following qualifications can apply:

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

Production Chemist – Freshers

Fresh graduates with B.Sc., M.Sc., B.Pharm. or M.Pharm. qualifications can apply for the Production Chemist position.

Production Chemist – Experienced Candidates

Candidates with up to 5 years of relevant experience in sterile, injectable or infusion manufacturing can apply.

Key Skills & Functional Areas

Sterile Infusion Manufacturing

The role involves manufacturing of sterile infusion products in:

• Parenteral
• FFS
• BFS
• Bottle Pack systems

Production Operations

Candidates should be familiar with production activities such as:

• Sterile manufacturing
• Injectable manufacturing
• Infusion manufacturing
• Production parameter monitoring
• Batch record maintenance
• Line clearance
• BMR / SOP compliance

Freshers Can Apply

Aculife Healthcare is specifically seeking motivated and detail-oriented freshers for the Production Department. Fresh graduates with the required educational qualifications can apply.

Job Location

Aculife Healthcare Private Limited

Location: Sanand – Viramgam region, Ahmedabad, Gujarat

The recruitment poster mentions the work location as the Aculife Healthcare facility near Sachana, Taluka – Viramgam, District Ahmedabad.

How to Apply

Interested candidates can attend the Aculife Healthcare Walk-In Interview on 03 October 2026, between 09:00 AM and 02:00 PM.

Candidates who are unable to attend the interview can send their CV by email.

CV Submission

Email: recruitment@aculife.co.in
Email: rajeshparmar@aculife.co.in

Candidates should share their updated CV with the recruitment team.

Job Summary

Ipca Laboratories Ltd., Dewas Unit II is looking for experienced professionals to join its Production Department. The current openings are for Sr. Officer, Officer and Technician positions. Candidates with relevant pharmaceutical industry experience can apply for roles in Granulation, Compression and Coating sections. Interested candidates can send their updated resume to the company for consideration.

Ipca Laboratories Ltd. – Production Department

Sr. Officer / Officer / Technician – Production

Department: Production
Sections: Granulation | Compression | Coating
Positions: Sr. Officer | Officer | Technician
Experience: Relevant Pharmaceutical Industry experience preferred
Location: Dewas Unit II

Production Department – Granulation

Sr. Officer / Officer / Technician

Candidates with relevant pharmaceutical manufacturing experience can apply for Production positions associated with the Granulation section.

Relevant experience in pharmaceutical production operations will be preferred.

Production Department – Compression

Sr. Officer / Officer / Technician

The opening also covers the Compression section within the Production Department.

Candidates with relevant experience in pharmaceutical manufacturing and compression operations can apply.

Production Department – Coating

Sr. Officer / Officer / Technician

The recruitment also includes opportunities in the Coating section.

Candidates with relevant pharmaceutical production experience are preferred.

Eligibility & Qualifications

The recruitment poster does not specify the educational qualification for the Sr. Officer, Officer and Technician positions.

For role-based eligibility, candidates with relevant pharmaceutical manufacturing backgrounds may be considered for the respective positions. Typical qualifications for these functions include:

B.Pharm | M.Pharm | Diploma in Pharmacy / Pharmaceutical Technology | ITI / Technical Diploma

Production – Sr. Officer / Officer

B.Pharm | M.Pharm or other relevant pharmaceutical qualifications.

Production – Technician

Diploma | ITI or other relevant technical qualifications.

Note: The above qualification guidance is based on the nature of the positions. Candidates should verify the exact eligibility requirements with Ipca Laboratories before applying.

Experience Required

Production Department

Relevant Pharmaceutical Industry experience preferred.

The recruitment poster does not mention a specific number of years of experience.

Candidates with relevant experience in pharmaceutical manufacturing and Production operations can apply.

Key Functional Areas

Granulation

Experience in pharmaceutical manufacturing operations related to Granulation is relevant.

Compression

Experience in tablet compression and manufacturing operations is relevant.

Coating

Experience in tablet coating and related pharmaceutical production operations is relevant.

Job Location

Ipca Laboratories Ltd. – Dewas Unit II

Location: Dewas Unit II

How to Apply

Interested candidates can share their updated resume with Ipca Laboratories Ltd.

Resume Submission

Email: preeti.upadhyay@ipca.com

Candidates are requested to mention the Department, Section and Designation applied for in the subject line of the email.

For example:

Production – Granulation – Officer

or

Production – Compression – Technician

Job Summary

Bioagile Therapeutics Clinical Research Associate (CRA) Recruitment

Bioagile Therapeutics is hiring a Clinical Research Associate (CRA) for its Clinical Operations team.
The opportunity is suitable for professionals with 1–2 years of experience in CRA, CRC, or CTA roles.
The role involves supporting clinical trials from study start-up through close-out, site monitoring, documentation, and regulatory compliance.
Candidates interested in building their career in clinical research and CRO operations can apply by sharing their CV with the recruitment team.

Clinical Research Associate (CRA) – Clinical Operations

Job Overview

Company: Bioagile Therapeutics
Position: Clinical Research Associate (CRA)
Department: Clinical Operations
Experience: 1–2 years in CRA / CRC / CTA roles
Work Environment: Clinical Research / CRO

Job Role & Responsibilities

Clinical Trial Operations

The Clinical Research Associate will be responsible for supporting clinical trial activities throughout the study lifecycle, including:

• Supporting clinical trial activities from study start-up through close-out.
• Conducting and supporting site monitoring activities.
• Ensuring compliance with:

  • Study protocols
  • Good Clinical Practice (GCP)
  • Applicable regulatory requirements

• Maintaining essential study documentation and trial records.
• Coordinating with investigators, clinical trial sites, and internal teams.
• Supporting effective communication between study stakeholders.
• Contributing to the smooth execution of clinical operations activities.

Eligibility & Qualifications

Experience

1–2 years of experience in CRA, CRC, or CTA roles

Candidates with hands-on exposure to clinical research operations, site coordination, clinical trial documentation, or monitoring activities would be relevant to the position.

Educational Qualification

The provided recruitment source does not specify a mandatory educational qualification.

For candidates looking to match the role, relevant backgrounds may include:

B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences | Clinical Research-related qualifications

These are role-aligned qualification examples and are not stated as mandatory requirements in the provided source.

Eligible Qualification Courses

B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences

Key Clinical Research Skills

Relevant areas for the position include:

• Clinical Research
• Clinical Operations
• Clinical Trial Management
• Site Monitoring
• Site Coordination
• Study Start-Up
• Study Close-Out
• GCP Compliance
• Clinical Trial Documentation
• Regulatory Compliance
• Investigator Coordination
• Clinical Site Management

Job Location & Details

Company: Bioagile Therapeutics

Position: Clinical Research Associate (CRA)

Department: Clinical Operations

Experience: 1–2 years in CRA / CRC / CTA roles

Industry: Clinical Research / CRO

How to Apply

Interested candidates can share their updated CV with Bioagile Therapeutics at:

Email: hr@bioagiletherapeutics.com

Candidates are encouraged to mention their relevant CRA, CRC, or CTA experience when applying.

Job Summary

Lilly Scientific Writer / Senior Scientific Writer – Quality Review & Document Finalization

Lilly is hiring a Scientific Writer / Senior Scientific Writer – Quality Review and Document Finalization for its Research & Development team in Bangalore, Karnataka.
The role focuses on producing high-quality scientific and medical regulatory documents, with responsibility for grammar, formatting, data accuracy, consistency, and document quality review.
The position also involves eCTD-compliant PDF production, Word document review, regulatory document publishing, and final quality checks.
Candidates with a Bachelor’s degree and strong scientific writing, communication, analytical, project management, and document-processing skills can apply.

Scientific Writer / Senior Scientific Writer – Quality Review & Document Finalization

Job Overview

The Scientific Writer / Senior Scientific Writer will support Lilly’s Global Scientific Communications team and other functions in producing accurate, high-quality documents that meet international standards.

The role combines scientific document quality review, editing, formatting, data verification, and regulatory document finalization.

Job ID: R-112204
Location: Bangalore, Karnataka, India
Category: Research & Development
Employment Type: Full Time, Regular

Scientific Communications Document Support

The role includes:

• Ensure timely delivery of error-free, high-quality documents that meet international standards of written English.
• Correct errors relating to:

  • Grammar
  • Style
  • Formatting
  • Syntax

• Identify and correct flaws in logic and document flow.
• Follow style guides and templates provided by the team.
• Follow best practices based on Lilly internal standards.
• Verify data against source files.
• Ensure accuracy and consistency of data and content within and between related documents.

Document Finalization & Publishing

The Scientific Writer / Senior Scientific Writer will also support regulatory document publishing activities:

• Produce final eCTD-compliant PDFs of medical regulatory documents using publishing software.
• Review and format Word files to ensure regulatory compliance requirements are incorporated into the source file wherever possible.
• Render Word files into PDF format.
• Review generated PDFs.
• Edit PDFs as required to ensure applicable regulatory requirements are met.

General Responsibilities

The role requires the ability to:

• Maintain a strong customer focus.
• Take accountability for achieving timelines.
• Manage activities efficiently and proactively.
• Understand and apply team communication strategies to work products.
• Coach new staff or colleagues requiring development in core areas.
• Coordinate with vendors when relevant activities are outsourced.

Process Efficiency & Technology

The position also involves process improvement and technology-related activities:

• Maintain proficiency in applicable software, tools, processes, and workflows.
• Introduce new tools, processes, and structures where appropriate to support organizational goals and standards.
• Develop solutions to streamline team workflows.
• Improve document processes by establishing uniform practices across the organization.
• Suggest process or tool enhancements to improve effectiveness.
• Help minimize redundancy between databases and other tools.

Therapeutic & Disease State Knowledge

The role requires an understanding of:

• Key priorities and communication strategies across therapeutic areas and organizational units.
• Product information.
• Disease-state information.
• Scientific and clinical knowledge relevant to assigned activities.
• Clinical trial design.
• Trial rationale and data.

The selected professional is expected to continue developing therapeutic knowledge and apply it to the responsibilities of the role.

Eligibility & Qualifications

Educational Qualification

Bachelor’s degree

The supplied job description does not specify a mandatory pharmacy, life sciences, or other particular bachelor’s specialization.

Minimum Qualification Requirements

Candidates should have:

• Strong written and verbal communication skills in English.
• Ability to communicate and negotiate solutions to complex technical challenges.
• Ability to work with:

  • Cross-functional colleagues
  • External vendors
  • Customers

• Demonstrated project management and time management skills.
• Strong verbal reasoning.
• Attention to detail.
• Critical thinking.
• Analytical ability.
• Interpersonal skills.
• Flexibility in varying work environments.
• High-level end-user computer skills, including:

  • Word processing
  • Tables and graphics
  • Spreadsheets
  • Presentations
  • Templates

• Ability to work independently and as part of a team.
• Ability to work across culturally and geographically diverse environments.
• Ability to assemble, share, and apply key learnings across multiple projects.

Eligible Qualification Courses

Bachelor’s Degree | B.Sc. Life Sciences | B.Pharm | B.Sc. Biotechnology | B.Sc. Biochemistry | Other Relevant Bachelor’s Degree

The source specifically requires a Bachelor’s degree; it does not specify these individual courses. The additional courses above are role-aligned examples rather than stated mandatory qualifications.

Additional Skills & Knowledge

The job posting also identifies the following as additional preferences:

• Knowledge of medical terminology.
• Knowledge of statistical terminology.
• Willingness to develop scientific knowledge.
• Ability to understand strategic issues.
• General knowledge of scientific literature search and retrieval.
• Strong document review and editing capabilities.
• Ability to work with scientific and medical information.

Travel Requirement

Limited travel: Up to approximately 10%.

Job Location & Details

Company: Eli Lilly and Company

Position: Scientific Writer / Senior Scientific Writer – Quality Review and Document Finalization

Job ID: R-112204

Location: Bangalore, Karnataka, India

Department: Research & Development

Employment Type: Full Time, Regular

Work Area: Scientific Communications / Medical Regulatory Documentation

How to Apply

Interested and eligible candidates can apply through the official Lilly Careers portal.

Apply Now – Lilly Scientific Writer / Senior Scientific Writer

Job Summary