Author: Sudheer vanguri

Bioagile Therapeutics Pvt. Ltd. is hiring a Clinical Research Associate (CRA) to join its clinical research team.
The company is looking for candidates with 1–2 years of experience in CRA, CRC or CTA roles.
This opportunity is suitable for professionals with relevant clinical research experience seeking to continue their career in clinical operations.
Interested candidates can share their updated CV directly with the company for consideration.

Bioagile Therapeutics – Clinical Research Department

Clinical Research Associate (CRA)

Experience: 1–2 Years
Relevant Experience: CRA / CRC / CTA

The selected candidate will be part of the clinical research function and support clinical trial activities according to the requirements of the role.

Eligibility & Qualifications

Bioagile Therapeutics – CRA Qualification

The provided recruitment notice does not specify an educational qualification. Candidates with relevant qualifications in Pharmacy, Life Sciences, Biotechnology, Medicine or related clinical research disciplines may be considered based on their experience.

B.Pharm | M.Pharm | Pharm.D | MBBS | B.Sc. Life Sciences | M.Sc. Life Sciences | Biotechnology | Clinical Research

Experience Requirements

• 1–2 years of professional experience in Clinical Research.
• Experience in CRA, CRC or CTA roles is required.
• Candidates should have relevant exposure to clinical research or clinical trial operations.

How to Apply

Interested candidates can send their CV to:

hr@bioagiletherapeutics.com

Candidates should include the Clinical Research Associate (CRA) position in the email subject line.

Job Summary

Virchow Biotech Private Limited is hiring a Senior Executive – Regulatory Affairs for its regulatory team.
The role focuses on National Regulatory Affairs, CDSCO and State FDA / DCA submissions.
Candidates with pharmaceutical regulatory affairs experience and prior r-DNA regulatory experience can apply.
The position requires 3–6+ years of experience, with M.Pharm in Regulatory Affairs preferred.

Virchow Biotech – Regulatory Affairs Department

Senior Executive – Regulatory Affairs

Department: Regulatory Affairs
Area: National Regulatory, CDSCO & State FDA / DCA
Experience: 3–6+ Years in Pharmaceutical Regulatory Affairs
Salary: As per present package
Location: Hyderabad, Telangana

Scope of Work – Regulatory Affairs

Scope 01: Regulatory Submissions

• Registrations & renewals
• Variations & amendments
• Licences & permissions
• NOC applications

Scope 02: Regulatory Compliance

• CDSCO & State FDA filings
• Deficiency responses
• Label & artwork review
• Audit & inspection support

Eligibility & Qualifications

Educational Qualifications

B.Pharm | M.Pharm | M.Pharm in Regulatory Affairs

M.Pharm in Regulatory Affairs is preferred for the position.

Experience Requirements

• 3–6+ years of experience in pharmaceutical Regulatory Affairs.
• Previous r-DNA regulatory experience is mandatory.
• Experience with ODLS, NSWS, CDSCO Sugam, CDSCO MD and ONDLS is required.
• Knowledge of Drugs & Cosmetics Rules, GMP and ICH requirements.

Required Regulatory Knowledge

Candidates should have relevant knowledge and experience in:

• r-DNA regulatory submissions
• CDSCO regulatory requirements
• State FDA / DCA requirements
• Regulatory registrations and renewals
• Variations and amendments
• Licences and permissions
• NOC applications
• Deficiency responses
• Label and artwork review
• Audit and inspection support
• Drugs & Cosmetics Rules
• GMP
• ICH requirements

Must-Have Requirement

Previous r-DNA regulatory experience is mandatory for this position.

Documents Required

Candidates are requested to bring the following documents:

• Updated CV
• One passport-size photograph
• Last three payslips
• Bank statement
• Increment letter
• Original educational and experience certificates
• Government photo identity proof

How to Apply

Interested candidates can send their updated CV to:

hr@virchowbiotech.com

Candidates should mention “Sr. Executive – Regulatory Affairs” in the subject line of the email.

Contact Details

Phone: +91 91001 25845
Email: hr@virchowbiotech.com

Walk-In / Interview Venue

Virchow Biotech Private Limited
Unit – I, Gagillapur,
Hyderabad – 500043, Telangana.

Only shortlisted candidates will be contacted.

Job Summary

Exemed Pharmaceuticals is hiring experienced professionals for multiple functions in its pharmaceutical API manufacturing operations.
The company has openings across R&D Documentation, QA, Quality Control, Microbiology, Electrical and Process Engineering departments.
Candidates with relevant pharmaceutical, chemistry, microbiology and engineering qualifications can apply for the available positions.
The openings require 2–9 years of experience, depending on the role and department.

Exemed Pharmaceuticals – R&D Department

Executive – R&D Documentation

Experience: 5–7 Years
Qualification: M.Sc. Organic Chemistry
Department: R&D

Key Responsibilities

• Prepare, review and maintain R&D documentation, including SOPs, STPs, protocols and reports.
• Ensure data integrity and compliance with cGMP / GLP.
• Support development reports, stability studies and regulatory submissions such as DMF/CTD.

Exemed Pharmaceuticals – Quality Assurance Department

Executive – AQA

Experience: 5–7 Years
Qualification: M.Sc.
Department: QA

Key Responsibilities

• Review and approve analytical documents, including SOPs, STPs and test methods.
• Ensure compliance with GMP, cGMP and regulatory requirements.
• Handle laboratory investigations, OOS/OOT and change controls.
• Support audits and regulatory inspections.

Exemed Pharmaceuticals – Quality Control Department

Officer – HPLC

Experience: 3–5 Years
Qualification: B.Sc. or M.Sc.
Department: Quality Control (QC)

Key Responsibilities

• Operate and analyze samples on HPLC, including method validation and routine analysis.
• Maintain HPLC instruments and Chromeleon / relevant software.
• Ensure data integrity and compliance with GMP requirements.
• Prepare analytical reports and support regulatory audits.

Exemed Pharmaceuticals – Microbiology Department

Officer – Microbiologist

Experience: 3–5 Years
Qualification: M.Sc.
Department: Microbiology (QC/QA)

Note: Male candidate required.

Key Responsibilities

• Conduct microbiological analysis of raw materials, intermediates and finished products.
• Perform microbial limits, bioburden and environmental monitoring.
• Maintain documentation as per GMP requirements.
• Support method validation and laboratory compliance.

Exemed Pharmaceuticals – Engineering / Maintenance Department

Electrician

Experience: 2–5 Years
Qualification: ITI (Electrician)
Department: Engineering / Maintenance

Key Responsibilities

• Troubleshoot and maintain electrical systems and equipment.
• Perform preventive and breakdown maintenance of plant utilities.
• Ensure safety and compliance with electrical standards.
• Support installation, testing and commissioning of electrical equipment.

Exemed Pharmaceuticals – Process Engineering Department

Senior Executive – Process Engineering

Experience: 7–9 Years
Qualification: B.E. Chemical
Department: Process Engineering

Note: Pharma API experience required.

Key Responsibilities

• Handle process engineering activities for API manufacturing.
• Manage process optimization, scale-up, troubleshooting and debottlenecking.
• Prepare and review process documents, PFD, P&ID and SOPs.
• Support technology transfer, new product commercialization and regulatory compliance.

Eligibility & Qualifications

Educational Qualifications

M.Sc. Organic Chemistry | M.Sc. | B.Sc. | ITI Electrician | B.E. Chemical

Candidates should have the relevant educational qualification and experience required for the respective position.

Experience Requirements

• Executive – R&D Documentation: 5–7 Years
• Executive – AQA: 5–7 Years
• Officer – HPLC: 3–5 Years
• Officer – Microbiologist: 3–5 Years
• Electrician: 2–5 Years
• Senior Executive – Process Engineering: 7–9 Years

How to Apply

Interested candidates can send their updated CV to:

recruitment@exemedpharma.com

Application Details

Candidates should mention the position and department they are applying for in the subject line of the email to help the recruitment team identify the application correctly.

Job Location

Exemed Pharmaceuticals
Block No. 628 A&B, ECP Canal Road,
At & Po – Luna, Ta – Padra,
Dist – Vadodara, Gujarat.

Job Summary

Pontika Aerotech is conducting a Walk-In Drive for experienced professionals across multiple pharmaceutical departments.
The company has openings in Packing, Production, Quality Control and Warehouse functions.
Candidates with relevant pharmaceutical, science, ITI, 10th, 12th and graduate qualifications can apply for the available positions.
The recruitment covers multiple dosage forms and manufacturing areas, including Aerosol, Nasal, Semisolid, Liquid, Cream, Tablet, Capsule and Injectable operations.

Pontika Aerotech – Packing Department

Officer / Executive – Packing

Experience: 1–8 Years
Qualification: B.Sc. / B.Pharma / D.Pharma / M.Pharma

The position is associated with packing operations across pharmaceutical dosage forms.

Pontika Aerotech – Packing / Production Department

Operators – Packing / Production

Experience: 1–8 Years
Qualification: ITI / 10th / 12th

Candidates can be considered for packing and production operations involving the listed dosage forms and manufacturing areas.

Pontika Aerotech – Production Department

Officer / Executive – Production

Experience: 1–6 Years
Qualification: B.Sc. / B.Pharma / M.Pharma

The production openings cover pharmaceutical manufacturing operations across multiple dosage forms.

Pontika Aerotech – Quality Control Department

Officer / Executive – Quality Control

Experience: 1–8 Years
Qualification: B.Sc. / M.Sc. / M.Pharma

The Quality Control positions cover all QC sections and include opportunities across the listed pharmaceutical dosage forms.

Pontika Aerotech – Warehouse Department

Officer / Executive – Warehouse

Experience: 1–8 Years
Qualification: Any Graduate

The Warehouse position involves RM dispensing and receiving activities.

Dosage Forms & Manufacturing Areas

Pontika Aerotech – Dosage Forms

The recruitment covers the following dosage forms:

• Aerosol
• Nasal
• Semisolid
• Liquid
• Cream
• Tablet
• Capsule
• Injectable

Pontika Aerotech – Production & Packing Areas

Relevant manufacturing areas include:

• Autoclave
• Filling
• Labelling
• Autocartoner
• Packing

Pontika Aerotech – Quality Control Areas

The Quality Control opportunity covers:

• Aerosol
• Nasal
• Semisolid
• Liquid
• Cream & Injectable
• All QC Sections

Eligibility & Qualifications

Educational Qualifications

B.Sc. | M.Sc. | B.Pharma | M.Pharma | D.Pharma | Any Graduate | ITI | 10th | 12th

Candidates should meet the qualification and experience requirements specified for the respective position.

Experience Requirements

• Packing – Officer / Executive: 1–8 Years
• Packing / Production – Operators: 1–8 Years
• Production – Officer / Executive: 1–6 Years
• Quality Control – Officer / Executive: 1–8 Years
• Warehouse – Officer / Executive: 1–8 Years

How to Apply

Interested candidates can apply via WhatsApp at:

8278729004

Walk-In Interview Details

Date: 27 September 2026
Time: 10:00 AM to 3:00 PM
Location: Paonta Sahib, Himachal Pradesh
Venue: Pontika Aerotech

Candidates should carry their updated resume and relevant educational and experience documents for the interview.

Job Summary

Marksans Pharma Ltd is hiring professionals for its Quality Assurance Department under the IPQA section.
The opening is for Officer / Sr. Officer positions for candidates with relevant pharmaceutical quality experience.
Candidates holding B.Pharm or M.Pharm qualifications and 2–5 years of experience can apply.
Immediate joiners are preferred for this Quality Assurance opportunity.

Marksans Pharma – Quality Assurance Hiring

Officer / Sr. Officer – Quality Assurance | Marksans Pharma

Department: Quality Assurance
Section: IPQA
Experience: 2–5 Years
Qualification: B.Pharm / M.Pharm
Preference: Immediate joiners preferred

The position is within the In-Process Quality Assurance (IPQA) function and is suitable for candidates with relevant pharmaceutical quality assurance experience.

Eligibility & Qualifications

Educational Qualification

B.Pharm | M.Pharm

Candidates with a relevant pharmaceutical qualification and experience in Quality Assurance / IPQA can apply.

Experience Required

2–5 Years

Relevant experience in pharmaceutical Quality Assurance and IPQA is applicable to the advertised position.

How to Apply

Interested candidates can share their updated resume with:

Email: muskan.shaikh@marksanspharma.com

Candidates should include their relevant qualification, experience and current availability in their resume.

Job Summary

Veedo Lifesciences is hiring freshers for its Bioanalytical Research team through a walk-in drive.
The available roles include Analyst, BQM and Custodian, offering opportunities for candidates with pharmaceutical and life sciences qualifications.
The roles involve sample analysis, analytical data review, laboratory documentation and proper handling of biological samples and laboratory materials.
Candidates with B.Pharm, M.Pharm or M.Sc. qualifications can attend the walk-in drive in Ahmedabad.

Veedo Lifesciences – Analyst, BQM & Custodian

Analyst – Bioanalytical Research | Veedo Lifesciences

The Analyst role involves sample collection, sample processing and analytical testing as part of bioanalytical research activities.

Role & Responsibilities

• Collect samples for analysis from the custodian.
• Process samples using various sample extraction techniques to determine the concentration of analyte.
• Perform analysis via LCMS.
• Follow GXP requirements during analytical activities.

BQM – Bioanalytical Research | Veedo Lifesciences

The BQM role involves reviewing analytical data and laboratory documentation to support compliance and accuracy.

Role & Responsibilities

• Review compiled data including MV, MD and study data.
• Review system and analytical laboratory equipment calibration records.
• Review equipment logbooks and preventive maintenance schedules.
• Verify documentation from the analyst/GL in accordance with respective SOPs.
• Review method SOPs, study plans and method validation protocols.
• Provide observation reports to the respective GL for correction purposes.

Custodian – Bioanalytical Research | Veedo Lifesciences

The Custodian role focuses on the appropriate handling, storage, documentation and disposal of laboratory materials.

Role & Responsibilities

• Ensure proper handling of biological samples, chemicals and laboratory materials.
• Maintain appropriate storage and documentation.
• Ensure proper disposal of biological samples, chemicals and laboratory materials.
• Follow GLP, GCP and applicable regulatory guidelines.

Eligibility & Qualifications

Veedo Lifesciences – Analyst, BQM & Custodian

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

Candidates with relevant pharmaceutical, life sciences or analytical laboratory backgrounds can apply for the available Bioanalytical Research positions.

Experience Requirements

The recruitment is specifically mentioned for Freshers.

Experience: Freshers

Walk-In Interview Details

Date: 27 September 2026, Sunday
Time: 10:00 AM to 2:00 PM

Venue – Veedo Lifesciences

Satyamev Corporate
Opp. Prahlad Nagar Fire Station
Near Shalin Bungalows
Corporate Road, Prahlad Nagar
Ahmedabad, Gujarat – 380015

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue mentioned above.

Candidates should carry their updated CV and relevant educational documents for the interview.

Job Summary

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