Author: Sudheer vanguri

Felix Generics Pvt. Ltd. is conducting a walk-in interview in Ahmedabad for multiple pharmaceutical manufacturing and quality positions at its Pithampur plant.
The recruitment drive includes openings in Injectable Production, Quality Control, Quality Assurance, Technology Transfer, Validation, and OSD Production.
Candidates with ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, or M.Sc. Chemistry qualifications can apply for relevant positions.
The walk-in interview is scheduled for 25 October 2026 at Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat.

Felix Generics Recruitment: Department-Wise Vacancies

Felix Generics Pvt. Ltd. is inviting applications from experienced pharmaceutical professionals for manufacturing, quality, validation, and technology transfer roles. The recruitment covers injectable and oral solid dosage (OSD) operations, with positions ranging from Technician and Officer to Assistant Manager and Deputy Manager.

Walk-In Interview Details

• Company: Felix Generics Pvt. Ltd.
• Recruitment Type: Walk-In Interview
• Interview Date: 25 October 2026, Sunday
• Interview Time: 9:30 AM to 3:30 PM
• Interview Location: Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054
• Plant Location: Pithampur
• Contact Numbers: 9109968673, 9109912946, 9109996408
• Resume Email: jobs@felixvet.com

1. Injectable Production Department

Available Positions

• Technician
• Senior Officer
• Executive

Eligibility & Qualifications

• ITI
• Diploma
• B.Pharm
• M.Pharm

Experience: 2–6 years for Technician, 4–5 years for Senior Officer, and 5–8 years for Executive.

Key Responsibilities

Technician

• Handle aseptic filling and filtration operations.
• Operate vial washing and autoclave equipment.
• Work in microsphere manufacturing and controlled areas.

Senior Officer

• Manage packing and labelling areas.
• Perform visual inspection activities.

Executive

• Handle aseptic area operations, including filling, filtration, and capping.

2. Quality Control Microbiology Department (Injectable)

Available Positions

Officer / Senior Executive

Eligibility & Qualifications

• M.Sc. Microbiology
• M.Sc. Biotechnology

Experience: 2–7 years

Key Responsibilities

• Perform microbiological testing, including sterility, BET, MLT, and GPT.
• Conduct method validations.
• Maintain QMS documentation and compliance.
• Support audit readiness, data integrity, and GMP-regulated laboratory operations.

3. Quality Control Department (Injectable)

Available Positions

Officer to Executive

Eligibility & Qualifications

• M.Sc. Chemistry
• M.Pharm
• B.Pharm

Experience: 2–8 years

Key Responsibilities

• Handle and calibrate analytical instruments such as HPLC, GC, FTIR, UV, auto-titrators, and KF equipment.
• Perform analysis of raw materials, water, finished products, and stability samples.

4. Quality Assurance Department (Injectable)

Available Positions

Officer to Senior Executive

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 2–8 years

Key Responsibilities

• Perform IPQA activities, including line clearance, sampling, and in-process checks.
• Handle AQL and media fills.
• Support aseptic supervision and batch record review.
• Conduct audit trail reviews and batch release activities.
• Manage document collection, issuance, retrieval, and archiving.
• Prepare and review SOPs.

Candidates should have a strong understanding of good manufacturing practices.

5. Technology Transfer Department (OSD)

Available Positions

Assistant Manager / Deputy Manager

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 10–14 years

Key Responsibilities

• Support technology transfer and process optimization.
• Perform validation activities.
• Apply knowledge of cGMP and regulatory guidelines.
• Prepare, review, and approve GMP documents, including SOPs, BMR/BPR, protocols, and reports.
• Handle change controls, risk assessments, QRM, deviations, and investigations.

6. Validation Department (OSD)

Available Positions

Officer to Deputy Manager

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 4–15 years

Key Responsibilities

• Handle greenfield project activities.
• Support equipment qualification and computer system validation.
• Work on HVAC and water system qualification.
• Support compressed air and nitrogen system qualification.
• Handle temperature mapping.

7. Quality Control Department (OSD)

Available Positions

Officer to Senior Executive

Eligibility & Qualifications

• M.Sc.
• M.Pharm
• B.Pharm

Experience: 4–7 years

Key Responsibilities

• Perform routine and non-routine quality control testing of raw materials, in-process samples, and finished products.
• Use analytical instruments and techniques, including HPLC, GC, UV, KF, potentiometers, IR, dissolution, and Malvern Mastersizer.
• Ensure compliance with SOPs, GLP, and regulatory standards.
• Perform method validation, verification, and transfer activities according to ICH guidelines.
• Prepare and review analytical method validation, verification, and transfer protocols.

8. Production Department (OSD)

Available Positions

• Executive (Granulation / Compression / Packing)
• Officer (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Packing)
• Technician (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Liquid Filling / Bottle Primary Packing)

Eligibility & Qualifications

• M.Pharm
• B.Pharm
• D.Pharm
• Diploma
• ITI

Experience Requirements

• Executive: 4–7 years
• Officer: 2–4 years
• Technician: 2–6 years

Key Responsibilities

Executive and Officer Roles

• Work in pharmaceutical OSD manufacturing operations.
• Support granulation, compression, coating, and packing activities.
• Follow manufacturing procedures and documentation requirements.

Technician Role

• Operate granulation equipment independently.
• Perform spraying and roll compaction activities.
• Handle liquid and paste manufacturing equipment.
• Work in primary bottle packing, liquid filling, and related operations.
• Follow machine operation, cleaning, changeover, and alarm-handling procedures.

Candidates should have exposure to an USFDA-approved or EUGMP-approved company. Experience with material handling, electronic batch records, SAP, machine alarms, QMS, deviations, change control, SOPs, daily reports, and manpower handling is relevant to the listed roles.

Eligibility & Qualifications: Quick Overview

Department	Qualifications	Experience
Injectable Production	ITI, Diploma, B.Pharm, M.Pharm	2–8 years, depending on position
QC Microbiology (Injectable)	M.Sc. Microbiology, M.Sc. Biotechnology	2–7 years
QC (Injectable)	M.Sc. Chemistry, M.Pharm, B.Pharm	2–8 years
QA (Injectable)	M.Pharm, B.Pharm	2–8 years
Technology Transfer (OSD)	M.Pharm, B.Pharm	10–14 years
Validation (OSD)	M.Pharm, B.Pharm	4–15 years
QC (OSD)	M.Sc., M.Pharm, B.Pharm	4–7 years
Production (OSD)	M.Pharm, B.Pharm, D.Pharm, Diploma, ITI	2–7 years, depending on position

How to Apply

Interested candidates can attend the walk-in interview at the venue mentioned below. Candidates who cannot attend can send their resumes to the recruitment email address provided in the advertisement.

Walk-In Interview Address

Pride Plaza Hotel
Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054.

Date: 25 October 2026
Time: 9:30 AM to 3:30 PM

Application by Email

Send your updated resume to jobs@felixvet.com.

Documents to Carry

• Updated resume
• Educational certificates
• Relevant experience documents
• Government-issued identity proof
• Supporting documents for relevant technical skills and training

Additional Requirements

• Candidates should have experience in an USFDA-approved company.
• Good communication skills are required.
• Candidates who cannot attend the interview may email their resumes to the recruitment address.
• Confirm the exact designation and department requirements before attending.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Felix Generics Pvt. Ltd. is conducting the recruitment drive for its Pithampur plant.

2. When is the walk-in interview scheduled?

The interview is scheduled for 25 October 2026, from 9:30 AM to 3:30 PM.

3. Where will the interview take place?

The venue is Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054.

4. Which qualifications are accepted?

The advertisement lists ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, and M.Sc. Chemistry for relevant roles.

5. What is the experience requirement?

The listed experience requirements range from 2 to 15 years, depending on the department and designation.

6. How can candidates apply if they cannot attend?

Candidates who cannot attend the walk-in interview can send their resumes to jobs@felixvet.com.

Job Summary

Category	Details
Company	Felix Generics Pvt. Ltd.
Vacancies	Technician, Officer, Senior Officer, Executive, Assistant Manager, Deputy Manager, Senior Executive
Required Education	ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, M.Sc. Chemistry
Experience	2–15 years, depending on the role

Torrent Pharmaceuticals Walk-In Interview for Production, Quality Control and Quality Assurance Jobs

Torrent Pharmaceuticals is inviting applications for multiple pharmaceutical manufacturing and quality-related positions at its Baddi, Himachal Pradesh, and Indrad, Gujarat, facilities.
The recruitment drive includes openings in Quality Control, Microbiology, Quality Assurance, Production, Engineering, and Supply Chain Management.
Candidates with B.Sc, M.Sc, B.Pharm, M.Pharm, B.E., and relevant ITI qualifications can apply for suitable positions based on their experience.
The walk-in interview is scheduled for 25 October 2026 at Torrent Pharmaceuticals Limited, Baddi, Himachal Pradesh, from 9:00 AM to 2:00 PM.

Torrent Pharmaceuticals Recruitment: Department-Wise Vacancies

Torrent Pharmaceuticals is hiring candidates for pharmaceutical manufacturing, laboratory testing, quality assurance, engineering, and production planning activities. The advertised openings cover both experienced professionals and eligible trainees.

1. Torrent Pharmaceuticals Baddi Recruitment

Position: Executive / Technical Assistant

Department: Quality Control

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

Experience: 2–7 years

Key Responsibilities and Required Skills

• Analysis of finished products, stability samples, and raw materials.
• Knowledge of analytical method validation, verification, and method transfer.
• Familiarity with HPLC, GC, UV spectroscopy, and other analytical instruments.
• Understanding of laboratory practices, documentation, and regulatory requirements.
• Knowledge of data integrity and troubleshooting.

How to Apply

Candidates who cannot attend the walk-in interview may send their resumes to:

Email: recruitmentbaddi@torrentpharma.com

2. Torrent Pharmaceuticals Panoli Recruitment

Job Location: Panoli, Ankleshwar, Gujarat

Quality Control (Formulation)

Designation: Officer / Executive

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

Experience: 1–7 years

Job Description: Experience in HPLC, GC, GLP, and analytical method validation.

Quality Control – Microbiology

Designation: Officer / Executive

Qualification: B.Sc / M.Sc (Microbiology)

Experience: 2–6 years

Job Description: Experience in microbiological method validation and media preparation.

Quality Assurance (OSD)

Designation: Officer / Executive

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

Experience: 1–5 years

Job Description: Experience in IPQA and OSD documentation.

Quality Assurance (Liquid)

Designation: Officer / Executive

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

Experience: 1–5 years

Job Description: Experience in IPQA and liquid manufacturing documentation.

Quality Assurance (Injectable)

Designation: Officer / Executive

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

Experience: 1–5 years

Job Description: Experience in IPQA documentation for injectable manufacturing.

Production – OSD Formulation

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 2–6 years

Job Description: Experience in pharmaceutical manufacturing and packing documentation.

Liquid (Oral) Manufacturing

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 1–6 years

Job Description: Experience in oral liquid manufacturing, packaging, and documentation.

Production (Injectable)

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 2–6 years

Job Description: Experience in LVP, SVP manufacturing, and aseptic packaging operations.

Supply Chain Management – Production Planning

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm / MBA

Experience: 2–6 years

Job Description: Material planning, inventory monitoring, and production planning activities.

Production (ITI)

Designation: Trainee Junior Officer

Qualification: ITI (2 years completed in any trade)

Experience: 0–5 years

Job Description: Work in OSD and injectable plants as an Operator or Technician.

Engineering – Formulation Instrumentation

Designation: Officer / Executive

Qualification: B.E. (Instrumentation)

Experience: 3–7 years

Job Description: Maintenance of plant machinery, calibration, and instrumentation for OSD and injectable plants.

Engineering – Formulation Mechanical

Designation: Officer / Executive

Qualification: B.E. (Mechanical)

Experience: 3–7 years

Job Description: Knowledge of OSD and injectable plant maintenance.

Engineering – Formulation Electrical

Designation: Officer / Executive

Qualification: B.E. (Electrical)

Experience: 3–7 years

Job Description: Electrical maintenance of formulation and injectable plants.

Eligibility & Qualifications

Candidates should possess the educational qualifications and relevant experience specified for their preferred department.

Qualifications mentioned in the recruitment advertisement:

B.Sc | M.Sc | B.Pharm | M.Pharm | MBA | B.E. (Instrumentation) | B.E. (Mechanical) | B.E. (Electrical) | ITI

Experience requirements vary by position, ranging from fresher-level eligibility for the Production (ITI) trainee role to 7 years for certain laboratory and engineering positions.

How to Apply

Interested candidates should attend the walk-in interview on 25 October 2026, Sunday, from 9:00 AM to 2:00 PM.

Walk-In Interview Venue

Torrent Pharmaceuticals Limited
Near Baddi University, Village – Bhud, Makhnu Majra, Tehsil – Baddi, District – Solan, Himachal Pradesh 173205.

Candidates unable to attend the Panoli recruitment drive may send their resumes to:

Email: NavneetKaur@torrentpharma.com

Documents to Carry

• Updated resume
• Educational certificates
• Relevant experience documents
• Government-issued identity proof

Candidates should confirm the applicable location and role requirements before attending.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Torrent Pharmaceuticals is conducting recruitment for Quality Control, Quality Assurance, Production, Microbiology, Engineering, and Supply Chain Management positions.

2. What is the walk-in interview date?

The interview is scheduled for 25 October 2026, Sunday.

3. Which qualifications are accepted?

The listed qualifications include B.Sc, M.Sc, B.Pharm, M.Pharm, MBA, B.E. in relevant engineering disciplines, and ITI.

4. Can freshers apply?

The Production (ITI) Trainee Junior Officer position lists an experience range of 0–5 years. Candidates should confirm the specific eligibility criteria before applying.

5. What is the experience requirement?

Experience requirements vary by position, ranging from 0–5 years for the Production (ITI) trainee role to 1–7 years for several technical positions.

6. Where is the Baddi interview venue?

The venue is Torrent Pharmaceuticals Limited, near Baddi University, Village Bhud, Makhnu Majra, Tehsil Baddi, District Solan, Himachal Pradesh 173205.

Job Summary

Category	Details
Company	Torrent Pharmaceuticals
Vacancies	Executive, Technical Assistant, Officer, Trainee Junior Officer
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm, MBA, B.E. (Instrumentation / Mechanical / Electrical), ITI
Experience	0–7 years, depending on the position

Syneos Health Recruitment – Drug Safety Specialist I / II

Syneos Health is hiring Drug Safety Specialist I / II professionals for its pharmacovigilance operations in Hyderabad and Gurugram, India. This full-time, permanent opportunity is suitable for candidates with 1–6 years of experience in drug safety, individual case safety report (ICSR) processing, and pharmacovigilance activities. The role involves processing spontaneous, clinical trial, and literature cases, performing medical coding and narrative writing, and ensuring compliance with global pharmacovigilance guidelines. Candidates with relevant Pharmacy, Medical, Dental, or Homeopathic qualifications can review the job requirements and apply.

Company Overview

Syneos Health is a contract research and healthcare services company operating in the clinical research and life sciences industry. The company supports clinical development and related healthcare activities, including drug safety and pharmacovigilance operations.

Job Details

Job Role & Responsibilities

The Drug Safety Specialist I / II will support end-to-end individual case safety report processing and pharmacovigilance activities.

Key responsibilities include:

• Perform end-to-end ICSR case processing for spontaneous, clinical trial, and literature cases.

• Execute accurate data entry activities, particularly during the initial phase of the role.

• Manage case workflows, including triage, data entry, coding, narrative writing, and submission readiness.

• Ensure compliance with global pharmacovigilance guidelines, standard operating procedures (SOPs), and applicable regulatory requirements.

• Perform quality checks on processed safety cases based on experience and performance.

Eligibility & Qualifications

Candidates with the following educational qualifications are listed in the job advertisement.

Undergraduate qualifications:

• BHMS – Bachelor of Homeopathic Medicine and Surgery.

• BDS – Bachelor of Dental Surgery.

• B.Pharm – Bachelor of Pharmacy, including Pharmaceutical Analysis and Quality Assurance specializations.

Postgraduate qualifications:

• M.Pharm – Master of Pharmacy.

• MDS – Master of Dental Surgery.

Candidates should verify the accepted qualification and specialization requirements in the original listing before applying.

Experience Requirements

• Experience range: 1–6 years.

• Relevant experience in drug safety, pharmacovigilance, or ICSR case processing is applicable to the role.

• Candidates should be familiar with safety case workflows and regulatory documentation.

Required Skills

The job advertisement highlights the following skills:

• Drug Safety

• Pharmacovigilance

• ICSR case processing

• Clinical trial case processing

• Literature case processing

• Narrative writing

• Case data entry and coding

• Case triage and submission readiness

• Quality checks and regulatory compliance

Job Locations

The position is listed for the following locations:

• Hyderabad, Telangana

• Gurugram, Haryana

The advertisement lists the role as full-time and permanent.

How to Apply

Interested candidates can review the complete job description and submit their application through Naukri.

Apply for Drug Safety Specialist I / II at Syneos Health

Applicants should highlight their pharmacovigilance experience, ICSR case processing skills, medical coding knowledge, and narrative writing experience in their resumes.

Job Summary

Granules India Limited is conducting a walk-in interview for Production and Packing positions at its manufacturing facility.
The recruitment drive is open for Operator and Executive roles across granulation, compression, coating, packing, and capsule filling operations.
Candidates with ITI, Diploma, D.Pharm, B.Sc, B.Pharm, M.Pharm, or M.Sc qualifications and 2–8 years of experience can apply.
The walk-in interview will take place on 25 October 2026 at Hotel HRJ Sarovar Portico, Regal Square, M.G. Road, Indore, Madhya Pradesh.

Granules India Walk-In Interview for Production & Packing Jobs

Granules India Limited is inviting candidates with pharmaceutical formulation manufacturing experience to attend a walk-in interview for Production and Packing roles in Indore. The openings cover multiple oral solid dosage (OSD) manufacturing operations, including granulation, compression, coating, blister packing, bottle packing, and capsule filling.

Walk-In Interview Details

• Company: Granules India Limited
• Department: Production and Packing
• Job Roles: Operator / Executive
• Interview Date: 25 October 2026, Sunday
• Interview Time: 9:30 AM to 1:00 PM
• Interview Venue: Hotel HRJ Sarovar Portico, Regal Square, M.G. Road, Indore, Madhya Pradesh 452003
• Contact Number: 08418696400
• Work Location: Granules India Ltd., Gagillapur, Hyderabad

Granules India Production and Packing Vacancies

1. Granulation / Wurster Coating

Position: Operator / Executive

Eligibility & Qualifications: ITI | Diploma | D.Pharm | B.Sc | B.Pharm | M.Pharm | M.Sc

Experience: 2–8 years

Required Equipment Knowledge:

• RMG
• FBP
• FBD
• Wurster coating
• Roll compactor
• Blender

2. Compression

Position: Operator / Executive

Eligibility & Qualifications: ITI | Diploma | D.Pharm | B.Sc | B.Pharm | M.Pharm | M.Sc

Experience: 2–8 years

Required Equipment Knowledge:

• Hata
• Fette
• Korsch
• Killian
• Cadmach

3. Coating

Position: Operator / Executive

Eligibility & Qualifications: ITI | Diploma | D.Pharm | B.Sc | B.Pharm | M.Pharm | M.Sc

Experience: 2–8 years

Required Equipment Knowledge:

• Ohara
• Glatt
• ACG Smart
• Sejong
• Gansons
• Bectochem
• Bohle Coater

4. Packing

Position: Operator / Executive

Eligibility & Qualifications: ITI | Diploma | D.Pharm | B.Sc | B.Pharm | M.Pharm | M.Sc

Experience: 2–8 years

Required Equipment Knowledge:

Blister Packing: Cartonator, Uhlmann, BQS, IMA PG, B45, Hicart.

Bottle Packing: CVC, Pharmapack, Countec, labelling machines, IMA A200, Cartonator.

5. Capsule Filling / Inspection

Position: Operator / Executive

Eligibility & Qualifications: ITI | Diploma | D.Pharm | B.Sc | B.Pharm | M.Pharm | M.Sc

Experience: 2–8 years

Required Equipment Knowledge:

• AF90T
• AF150T
• ZRO 200
• TTS
• Hartnett printing
• Band sealing
• ACG
• Checkweighers
• Sensum
• Tam Print
• Encapsulation
• Pressfit

Eligibility & Qualifications

Candidates should have a relevant qualification and practical experience in pharmaceutical formulation manufacturing.

Eligible Qualifications:

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

Experience Required: 2–8 years

Additional Eligibility Requirements

• Candidates currently working with Technical Contract Services or NAPS with formulation production experience are also eligible to attend.
• Candidates must have OSD formulation experience.
• Applicants should be willing to work in shift operations.
• Selected candidates may receive spot offers, subject to document submission.

How to Apply for Granules India Recruitment

Interested candidates should attend the walk-in interview with an updated resume and the required supporting documents.

Walk-In Interview Address

Hotel HRJ Sarovar Portico
Regal Square, M.G. Road, Indore, Madhya Pradesh 452003.

Date: 25 October 2026
Time: 9:30 AM to 1:00 PM

Documents Required

Candidates should carry photocopies of the following documents:

• Updated resume
• Latest increment letter
• Last three months’ payslips from the current organization
• Relieving and service certificates from previous organizations
• Educational documents
• Aadhaar card
• PAN card

For queries, contact 08418696400.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Granules India Limited is conducting the recruitment drive for Production and Packing positions.

2. Which positions are available?

The openings include Operator and Executive roles in granulation, Wurster coating, compression, coating, packing, capsule filling, and inspection.

3. What qualifications are required?

Candidates with ITI, Diploma, D.Pharm, B.Sc, B.Pharm, M.Pharm, or M.Sc qualifications can apply.

4. How much experience is required?

The recruitment advertisement specifies 2–8 years of experience.

5. Can candidates with contract manufacturing experience attend?

Yes. Candidates currently working with Technical Contract Services or NAPS who have formulation production experience are also eligible to attend.

6. What is the walk-in interview date and time?

The interview is scheduled for 25 October 2026, from 9:30 AM to 1:00 PM.

Job Summary

Category	Details
Company	Granules India Limited
Vacancies	Operator / Executive: Granulation, Wurster Coating, Compression, Coating, Packing, Capsule Filling / Inspection
Required Education	ITI, Diploma, D.Pharm, B.Sc, B.Pharm, M.Pharm, M.Sc
Experience	2–8 years

 

Syn thimed Labs is conducting a walk-in interview for manufacturing positions, including Assistant Officer, Officer, Senior Officer, and Trainee Associate.
Candidates with B.Sc, M.Sc, Diploma in Chemical Engineering, or B.Sc qualifications can apply for the relevant positions.
Experienced candidates with up to 6 years of experience and freshers are eligible for different openings, depending on the role.
The walk-in interviews will be held on 24 and 25 October 2026 at Hotel Mansarovar Paradise, Moradabad, Uttar Pradesh.

Synthimed Labs Walk-In Interview: Manufacturing Jobs

Synthimed Labs is inviting applications for manufacturing positions at its facility. The recruitment includes opportunities for experienced professionals in manufacturing and freshers interested in cleanroom manufacturing operations.

Walk-In Interview Details

• Company: Synthimed Labs
• Department: Manufacturing
• Interview Dates: 24 October 2026 and 25 October 2026
• Interview Timing:

  • 24 October 2026: 9:00 AM to 4:00 PM
  • 25 October 2026: 9:00 AM to 1:00 PM

• Venue: Hotel Mansarovar Paradise, Mansarovar Colony, Delhi Road, Moradabad
• Key Requirement: API background with knowledge of reactors, centrifuges, and batch charging. cGMP, BPR, and safety guidelines are required.

1. Assistant Officer / Officer / Senior Officer

Department

Manufacturing

Eligibility & Qualifications

• B.Sc
• M.Sc
• Diploma in Chemical Engineering

Experience: 0–6 years

Key Requirements

• API manufacturing background
• Knowledge of reactors and centrifuges
• Knowledge of batch charging
• Understanding of current Good Manufacturing Practices (cGMP)
• Knowledge of Batch Production Records (BPR)
• Compliance with safety guidelines

2. Trainee Associate

Department

Manufacturing (Cleanroom)

Eligibility & Qualifications

• B.Sc

Experience: Freshers

Role Overview

This position is intended for freshers interested in cleanroom manufacturing operations. Candidates should have the required educational qualification and an interest in pharmaceutical manufacturing practices.

How to Apply for Synthimed Labs Recruitment

Interested candidates can share their resumes through the contact details provided in the recruitment advertisement.

Contact Details

• Kaur Paramjeet: kaur.paramjeet@synthimed.com
• Astha Trivedi: astha.trivedi@synthimed.com
• Contact Numbers:

  • Paramjeet Kaur: 9815943533
  • Astha Trivedi: 8968374200

• Website: www.synthimed.com

Walk-In Interview Venue

Hotel Mansarovar Paradise
Mansarovar Colony, Delhi Road, Moradabad

Documents to Carry

• Updated CV or resume
• Educational certificates
• Relevant experience documents, if applicable
• Government-issued identity proof

Candidates should attend the interview on the date applicable to them and confirm any additional requirements with the recruitment contacts.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Synthimed Labs is conducting the recruitment drive for manufacturing positions.

2. Which positions are available?

The openings include Assistant Officer, Officer, Senior Officer, and Trainee Associate.

3. Can freshers apply?

Yes. Freshers can apply for the Trainee Associate position in Manufacturing (Cleanroom).

4. What qualifications are required?

B.Sc, M.Sc, and Diploma in Chemical Engineering are listed for the experienced manufacturing positions. B.Sc is listed for the Trainee Associate position.

5. What is the required experience?

The Assistant Officer, Officer, and Senior Officer positions require 0–6 years of experience. The Trainee Associate position is open to freshers.

6. Where will the interview take place?

The interview venue is Hotel Mansarovar Paradise, Mansarovar Colony, Delhi Road, Moradabad.

Job Summary

Category	Details
Company	Synthimed Labs
Vacancies	Assistant Officer / Officer / Senior Officer; Trainee Associate
Required Education	B.Sc, M.Sc, Diploma in Chemical Engineering
Experience	0–6 years; Freshers eligible for Trainee Associate

Alembic Pharmaceuticals Limited is conducting a walk-in drive for experienced professionals in Injectable Production, Injectable Packing & Visual Inspection, Quality Control, Quality Assurance, and Engineering Plant Maintenance.
The recruitment drive offers multiple positions, including Technical Officer, Junior Executive, Executive, Senior Executive, and Junior Executive / Executive in Engineering.
Candidates with ITI, Diploma, B.Pharm, M.Pharm, M.Sc, B.E., or B.Tech qualifications can apply for suitable positions based on their experience and technical skills.
The walk-in interview is scheduled for 25 October 2026 at Sanskriti Hall, Alembic City, Vadodara, Gujarat, from 9:00 AM to 3:00 PM.

Alembic Pharmaceuticals Walk-In Drive: Department-Wise Vacancies

Alembic Pharmaceuticals Limited is inviting applications from eligible candidates for manufacturing, packing, quality control, quality assurance, and engineering positions at its Vadodara facility. The recruitment focuses on pharmaceutical injectable manufacturing and related operations.

Walk-In Interview Details

• Company: Alembic Pharmaceuticals Limited
• Departments: Injectable Production, Injectable Packing & Visual Inspection, QC – Injectable, QA – Injectable, Engineering Plant Maintenance
• Interview Date: 25 October 2026 (Sunday)
• Interview Time: 9:00 AM to 3:00 PM
• Venue: Sanskriti Hall, Alembic City, Vadodara, Gujarat
• Registration: Pre-booking is encouraged through the QR code provided in the recruitment advertisement.

1. Injectable Production Department

Available Positions

Technical Officer / Junior Executive / Executive / Senior Executive

Eligibility & Qualifications

• ITI
• Diploma
• B.Pharm
• M.Pharm

Experience: 1–10 years

Key Skills

• Aseptic processing
• Autoclave operations
• Isolator handling
• Lyophilization

Key Responsibilities

• Operate injectable manufacturing equipment.
• Perform filtration, filling, and freeze-drying operations.
• Follow standard operating procedures (SOPs) and Quality Management System (QMS) standards.

2. Injectable Packing & Visual Inspection Department

Available Positions

Technical Officer / Junior Executive / Executive / Senior Executive

Eligibility & Qualifications

• ITI
• Diploma
• B.Pharm
• M.Pharm

Experience: 1–8 years

Key Skills

• Aseptic packing
• Line clearance
• Documentation
• Visual inspection
• Batch record review

Key Responsibilities

• Operate packing lines for injectable products.
• Perform visual inspection, label checks, and batch documentation.
• Follow SOPs and current Good Manufacturing Practice (cGMP) guidelines.

3. Quality Control (QC) – Injectable Department

Available Positions

Technical Officer / Junior Executive / Executive / Senior Executive

Eligibility & Qualifications

• M.Sc
• B.Pharm
• M.Pharm

Experience: 2–5 years

Key Skills

• HPLC
• GC
• Analytical instruments
• Data integrity

Key Responsibilities

• Conduct analytical testing of injectable products.
• Maintain laboratory documentation.
• Ensure compliance with cGMP, Good Laboratory Practice (GLP), and data integrity requirements.

4. Quality Assurance (QA) – Injectable Department

Available Positions

Technical Officer / Junior Executive / Executive / Senior Executive

Eligibility & Qualifications

• M.Sc
• B.Pharm
• M.Pharm

Experience: 2–7 years

Key Skills

• In-Process Quality Assurance (IPQA)
• Line clearance
• Batch documentation
• Cleanroom monitoring
• cGMP compliance

Key Responsibilities

• Perform IPQA activities, including shop-floor monitoring, line clearance, and batch documentation.
• Ensure compliance with cGMP, aseptic practices, and sterile manufacturing requirements.

5. Engineering Plant Maintenance Department

Available Positions

Junior Executive / Executive (Pharma experience only)

Eligibility & Qualifications

• ITI
• Diploma
• B.E.
• B.Tech

Experience: 1–6 years

Key Responsibilities

Mechanical

• Preventive and breakdown maintenance of OSD and injectable machines.

Electrical

• HT/LT substation operations.

HVAC

• Preventive maintenance of HVAC systems.

Instrumentation

• Maintenance of control and instrumentation systems for OSD and injectable operations.

Eligibility & Qualifications: Quick Overview

Department	Eligible Qualifications	Experience
Injectable Production	ITI, Diploma, B.Pharm, M.Pharm	1–10 years
Injectable Packing & Visual Inspection	ITI, Diploma, B.Pharm, M.Pharm	1–8 years
QC – Injectable	M.Sc, B.Pharm, M.Pharm	2–5 years
QA – Injectable	M.Sc, B.Pharm, M.Pharm	2–7 years
Engineering Plant Maintenance	ITI, Diploma, B.E., B.Tech	1–6 years

How to Apply for Alembic Pharmaceuticals Recruitment

Interested candidates should pre-book their interview slots using the QR code displayed in the recruitment advertisement. Candidates should attend the walk-in interview with an updated CV and relevant documents.

Walk-In Interview Address

Sanskriti Hall, Alembic City, Vadodara, Gujarat

Date: 25 October 2026
Time: 9:00 AM to 3:00 PM

Documents to Carry

• Updated CV or resume
• Educational certificates
• Relevant work experience documents
• Government-issued identity proof
• Other supporting documents relevant to the applied position

Candidates should ensure they meet the qualification and experience requirements for their preferred department before attending the interview.

Frequently Asked Questions

1. Which company is conducting the walk-in drive?

Alembic Pharmaceuticals Limited is conducting the recruitment drive for Injectable Production, Packing, QC, QA, and Engineering positions.

2. What is the walk-in interview date?

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

3. Where will the interview take place?

The interview venue is Sanskriti Hall, Alembic City, Vadodara, Gujarat.

4. Which qualifications are accepted?

ITI, Diploma, B.Pharm, M.Pharm, M.Sc, B.E., and B.Tech qualifications are accepted for different positions, depending on the department.

5. Can freshers apply?

The advertisement specifies experience requirements ranging from 1 to 10 years for the listed positions. It does not explicitly identify these vacancies as fresher positions.

6. What is the interview timing?

The walk-in interview will take place from 9:00 AM to 3:00 PM.

Job Summary

Category	Details
Company	Alembic Pharmaceuticals Limited
Vacancies	Technical Officer, Junior Executive, Executive, Senior Executive, Engineering Junior Executive / Executive
Required Education	ITI, Diploma, B.Pharm, M.Pharm, M.Sc, B.E., B.Tech
Experience	1–10 years, depending on the department

Beta Drugs Limited is inviting applications for multiple pharmaceutical jobs at its manufacturing facility in Baddi, Himachal Pradesh.
The openings span Microbiology, Production OSD, Production Injection, Quality Assurance (QA), Quality Control (QC), Engineering, and Apprentice Trainee positions.
Eligible candidates with B.Tech, M.Sc, B.Pharm, M.Pharm, B.Sc, ITI, or Diploma qualifications can apply for relevant roles.
The recruitment includes opportunities for experienced professionals with 2–10 years of experience as well as freshers applying for Apprentice Trainee positions.

Beta Drugs Limited Recruitment: Department-Wise Job Vacancies

Beta Drugs Limited is expanding its workforce across pharmaceutical manufacturing, quality control, quality assurance, microbiology, and engineering operations. Candidates with relevant qualifications and experience can apply for the available positions at the Baddi facility.

Job Overview

• Company: Beta Drugs Limited
• Location: Baddi, Himachal Pradesh
• Departments: Microbiology, Production OSD, Production Injection, Quality Assurance, Quality Control, Engineering, and Apprentice Training
• Application Email: hr.baddi@betadrugslimited.com
• Contact Number: 9877798724

Department-Wise Vacancies at Beta Drugs Limited

1. Microbiology Department

Designation: Jr. Officer
Role: MLT, EM
Qualification: B.Tech / M.Sc
Experience: 2–3 years
Vacancies: 1

2. Production OSD Department

Operator – Capsule Filling

• Qualification: ITI / Diploma
• Experience: 3–5 years
• Vacancies: 1

Executive / Senior Executive – QMS Activity

• Qualification: B.Pharm / M.Pharm
• Experience: 6–8 years
• Vacancies: 1

3. Production Injection Department

Designation: Operator
Role: Lyophilized Operator
Qualification: ITI / Diploma
Experience: 4–8 years
Vacancies: 1

4. Quality Assurance (QA) Department

Officer / Senior Officer – Qualification & Validation

• Qualification: B.Pharm
• Experience: 4–8 years
• Vacancies: 1

Executive / Senior Executive – IPQA Injection

• Qualification: B.Pharm / M.Pharm
• Experience: 6–8 years
• Vacancies: 1

Officer / Senior Officer – IPQA Injection & IPQA OSD

• Qualification: B.Pharm / M.Pharm
• Experience: 3–5 years
• Vacancies: 2

Executive – QMS Activity

• Qualification: B.Pharm / M.Pharm
• Experience: 6–8 years
• Vacancies: 2

5. Quality Control (QC) Department

Senior Officer / Executive – Reviewer

• Qualification: B.Sc / M.Sc
• Experience: 6–10 years
• Vacancies: 2

Officer / Senior Officer – Analyst HPLC / AMV

• Qualification: B.Sc / M.Sc
• Experience: 2–5 years
• Vacancies: 3

6. Engineering Department

Designation: Technician
Role: Water System
Qualification: ITI / Diploma
Experience: 5–8 years
Vacancies: 1

7. Apprentice Trainee Vacancies

Beta Drugs Limited also lists apprentice opportunities for freshers.

Production Injection Apprentice Trainee

• Qualification: B.Pharm
• Vacancies: 1

Production Injection / OSD / Engineering Apprentice Trainee

• Qualification: ITI / Diploma
• Vacancies: 5

Eligibility & Qualifications

Educational Qualifications

Candidates with the following qualifications can apply for suitable positions:

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

Applicants should select positions based on the qualifications and experience specified for each department.

Experience Requirements

Experience requirements vary by role:

• Microbiology: 2–3 years
• Production OSD: 3–8 years, depending on the position
• Production Injection Operator: 4–8 years
• QA: 3–8 years, depending on the position
• QC Reviewer: 6–10 years
• QC Analyst HPLC / AMV: 2–5 years
• Engineering Technician: 5–8 years
• Apprentice Trainees: Freshers

Location & Salary

• Job Location: Baddi, Himachal Pradesh
• Salary: Not specified in the recruitment announcement.

Candidates can contact the recruitment team to obtain salary details and other employment terms.

How to Apply

Interested candidates can submit their updated resumes to Beta Drugs Limited by email.

Application Email: hr.baddi@betadrugslimited.com
Contact Number: 9877798724

Applicants should mention the position they are applying for and highlight their relevant educational qualifications and experience.

Documents Required

Candidates should keep the following documents ready:

• Updated resume or CV
• Educational qualification certificates
• Relevant work experience certificates, where applicable
• ITI or Diploma certificates for technical positions
• Supporting documents requested by the recruitment team

Frequently Asked Questions

1. Which company is hiring?

Beta Drugs Limited is recruiting for multiple positions at its Baddi facility.

2. Which departments have vacancies?

The openings include Microbiology, Production OSD, Production Injection, QA, QC, Engineering, and Apprentice Training.

3. Can freshers apply?

Yes. Freshers can apply for the listed Apprentice Trainee positions.

4. Which qualifications are accepted?

The listed qualifications include B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, ITI, and Diploma, depending on the role.

5. How can candidates apply?

Candidates can email their resumes to hr.baddi@betadrugslimited.com or contact 9877798724.

6. Where are the vacancies located?

The vacancies are based in Baddi, Himachal Pradesh.

Job Summary

Category	Details
Company	Beta Drugs Limited
Vacancies	Jr. Officer, Operator, Executive, Senior Executive, Officer, Senior Officer, Reviewer, Analyst, Technician, Apprentice Trainee
Required Education	B.Tech, M.Sc, B.Sc, B.Pharm, M.Pharm, ITI, Diploma
Experience	Freshers to 10 years, depending on the position

Homi Bhabha Cancer Hospital & Research Centre Recruitment – Clinical Research Coordinator

Homi Bhabha Cancer Hospital & Research Centre (HBCHRC), Visakhapatnam, under Tata Memorial Centre, is conducting a walk-in interview for one Clinical Research Coordinator position on 28 October 2026. The recruitment is under a Research Capacity Building Grant Resonance project for an initial period of six months. Candidates with qualifications in Life Sciences, Pharmacy, Clinical Research, or specified medical and dental disciplines can apply, subject to the mandatory postgraduate diploma in Clinical Research where applicable. The position offers ₹27,000 per month, and candidates must be aged 35 years or below.

Organization Overview

Tata Memorial Centre’s Homi Bhabha Cancer Hospital & Research Centre, Visakhapatnam, is recruiting a Clinical Research Coordinator under its Research Capacity Building Grant Resonance project. The appointment is initially for six months.

Job Details

Eligibility & Qualifications

Candidates must meet one of the qualification pathways specified in the official recruitment notice:

• Graduation or Post Graduation in Life Sciences or Pharmacy, along with a Post Graduate Diploma in Clinical Research. The diploma in Clinical Research is mandatory for this pathway.

• BDS, BAMS, BUMS, or BHMS, along with a Post Graduate Diploma in Clinical Research. The diploma in Clinical Research is mandatory for this pathway.

• M.Sc. in Clinical Research or Pharm.D.

Experience Requirements

• One year of experience in the clinical research field is desirable.

• Candidates must have completed all required courses and have their course certificates available when attending the interview.

Age Limit

– Upper age limit: 35 years.

Job Location

The selected candidate will be based at:

Homi Bhabha Cancer Hospital & Research Centre (HBCHRC)

Aganampudi, Visakhapatnam, Andhra Pradesh – 530053.

Salary & Contract Duration

• Monthly remuneration: ₹27,000.

• Initial appointment period: Six months under the Research Capacity Building Grant Resonance project.

Walk-In Interview Details

Documents Required

Eligible candidates should attend the walk-in interview with the following documents:

• Bio-data or updated resume.

• Recent passport-size photograph.

• Photocopy of PAN card.

• Aadhaar card.

• Original educational certificates.

• One set of attested copies of all certificates.

Internal candidates must submit a No Objection Certificate (NOC) from their current Head of Department or Principal Investigator.

The notice states that an MCQ test will be conducted if there are more candidates, and eligible candidates will be shortlisted for the interview accordingly.

How to Apply

Eligible candidates can attend the walk-in interview directly at the HRD Department, 1st Floor, Homi Bhabha Cancer Hospital & Research Centre, Aganampudi, Visakhapatnam, on 28 October 2026 between 9:30 AM and 10:30 AM.

Candidates should ensure that all required course certificates are completed and available before attending.

For queries, contact the number provided in the official notice: 0891-2871, Extension 538.

Job Summary

West Coast Pharmaceuticals is inviting applications from freshers for the FDA Assistant position at its Sola, Ahmedabad, facility.
Candidates who completed B.Sc., M.Sc., or B.Pharm in 2026 or are graduating in 2027 are eligible to apply.
The opportunity is suitable for candidates looking to begin their careers in the pharmaceutical industry.
Interested applicants can contact the company through WhatsApp or submit their resumes by email.

West Coast Pharmaceuticals Recruitment for FDA Assistant

West Coast Pharmaceuticals is hiring freshers for the FDA Assistant position at its Sola facility in Ahmedabad, Gujarat. Candidates with B.Sc., M.Sc., or B.Pharm qualifications from the 2026–2027 batches can apply for this opportunity.

Job Details

• Company: West Coast Pharmaceuticals
• Department: FDA
• Designation: FDA Assistant
• Experience: Freshers
• Eligible Pass-Out Years: 2026–2027
• Job Location: Sola, Ahmedabad, Gujarat
• Working Hours: 9:00 AM to 7:00 PM
• Working Days: Monday to Saturday

Company Overview

West Coast Pharmaceuticals operates in the pharmaceutical industry and is inviting applications from eligible candidates beginning their professional careers. This opening provides an opportunity for recent graduates to explore an entry-level pharmaceutical position.

Job Role & Responsibilities

The recruitment announcement identifies the position as FDA Assistant but does not provide a detailed list of job responsibilities.

Candidates can contact the recruitment team to clarify the specific duties, department requirements, and other role-related details before applying.

Eligibility & Qualifications

Educational Qualifications

Candidates with the following qualifications are eligible to apply:

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

Experience Requirements

• Freshers can apply.
• Eligible pass-out years: 2026 and 2027.

Additional Requirements

• Candidates should be available to work from 9:00 AM to 7:00 PM.
• The stated working schedule is Monday to Saturday.
• Applicants should confirm the role-specific requirements with the recruitment team.

Location & Salary

• Job Location: Sola, Ahmedabad, Gujarat
• Working Hours: 9:00 AM to 7:00 PM, Monday to Saturday
• Salary: Not specified in the recruitment announcement.

Candidates can contact the company directly for salary details and other employment terms.

How to Apply

Interested candidates can apply for the FDA Assistant position by sending their resumes to the recruitment email address below.

• Email: hrdho@westcoastin.com
• WhatsApp / Contact: +91 98751 70543

Applicants should provide accurate educational details and mention their eligible pass-out year when contacting the recruitment team.

Documents Required

Candidates should keep the following documents ready:

• Updated resume or CV
• B.Sc., M.Sc., or B.Pharm educational certificates or available academic records
• Government-issued identity proof, if requested
• Other documents requested by the recruitment team

Frequently Asked Questions

1. Which company is hiring FDA Assistants?

West Coast Pharmaceuticals is recruiting FDA Assistants.

2. Can freshers apply for this position?

Yes. The recruitment announcement specifically welcomes freshers.

3. Which qualifications are eligible?

Candidates with B.Sc., M.Sc., or B.Pharm qualifications can apply.

4. Which pass-out years are eligible?

The announcement lists the 2026 and 2027 pass-out years.

5. What are the working hours?

The stated working hours are 9:00 AM to 7:00 PM, Monday to Saturday.

6. How can candidates apply?

Candidates can email their resumes to hrdho@westcoastin.com or contact the recruitment team at +91 98751 70543.

Job Summary

Category	Details
Company	West Coast Pharmaceuticals
Vacancies	FDA Assistant
Required Education	B.Sc. / M.Sc. / B.Pharm
Experience	Freshers; 2026–2027 pass-out years

SIRO is hiring an experienced Senior Regulatory Medical Writer for its regulatory medical writing team. Candidates with at least 4 years of relevant experience in authoring and quality checking regulatory documents are encouraged to apply.
The role requires expertise in clinical and regulatory writing, including Clinical Study Reports (CSRs), Investigator’s Brochures (IBs), and clinical trial protocols.
Applicants must have experience across 2–4 phases of clinical trials. Bioavailability/Bioequivalence (BA/BE) experience will not be considered for this opportunity.
The position offers hybrid working in Mumbai or remote working for candidates based outside the city, with preference for immediate joiners and candidates serving short notice periods.

SIRO Senior Regulatory Medical Writer Recruitment

Company Overview

SIRO is inviting applications from experienced professionals for the position of Senior Regulatory Medical Writer. This opportunity is suitable for candidates with a strong background in regulatory documentation, clinical research writing, document authoring, and quality control.

Job Details

• Company: SIRO
• Department: Regulatory Medical Writing
• Designation: Senior Regulatory Medical Writer
• Experience: Minimum 4 years
• Location: Mumbai, Maharashtra, or remote for candidates based outside Mumbai
• Work Mode: Hybrid or remote, depending on location
• Joining Preference: Immediate joiners or candidates with a short notice period

SIRO Senior Regulatory Medical Writer Job Role & Responsibilities

The recruitment announcement highlights regulatory document authoring, quality checking, and clinical trial experience as the main requirements for this position.

Key Responsibilities

• Author regulatory documents, including Clinical Study Reports (CSRs), Investigator’s Brochures (IBs), and clinical trial protocols.
• Perform quality control (QC) of regulatory medical writing documents.
• Review clinical and regulatory documentation for accuracy and quality.
• Apply knowledge of clinical research and regulatory documentation requirements.
• Support the preparation and review of documents associated with clinical trials.

Eligibility & Qualifications

Educational Qualifications

The recruitment announcement does not specify a mandatory educational qualification. Candidates should confirm the academic eligibility criteria with the recruitment team.

Experience Requirements

• Minimum 4 years of relevant experience in regulatory medical writing.
• Experience in authoring and quality checking regulatory documents.
• Clinical trial experience across 2–4 phases is mandatory.
• Bioavailability/Bioequivalence (BA/BE) experience will not be considered for this position.

Required Skills

Candidates should have:

• Strong regulatory medical writing skills.
• Experience preparing and reviewing CSRs, IBs, and clinical trial protocols.
• Knowledge of clinical research and regulatory documentation.
• Strong document review and quality-checking abilities.
• Excellent written communication skills.
• Attention to detail and the ability to maintain documentation quality.

Location & Work Mode

SIRO is considering candidates for the following work arrangements:

• Mumbai: Hybrid working arrangement.
• Candidates based outside Mumbai: Remote working option.

Candidates should clarify the applicable work arrangement with the recruitment team during the application process.

Salary & Benefits

The salary package and additional employment benefits have not been specified in the recruitment announcement. Candidates can contact the recruitment team for further details.

How to Apply

Interested candidates who meet the experience and clinical trial requirements can apply by emailing their updated CV to the recruitment contact below.

Application Email: vedanshi.hemani@siroclinpharm.com

Application Instructions

• Send an updated CV highlighting relevant regulatory medical writing experience.
• Include experience in authoring and QC of regulatory documents.
• Clearly mention clinical trial experience across the applicable trial phases.
• Mention your current notice period and earliest possible joining date.
• Confirm your preferred work arrangement, whether hybrid in Mumbai or remote from outside Mumbai.

Joining Preference

Immediate joiners and candidates with short notice periods are preferred.

Documents Required

Candidates should keep the following documents ready:

• Updated resume or CV.
• Educational qualification certificates.
• Relevant work experience certificates.
• Supporting details of regulatory document authoring and QC experience.
• Details of clinical trial experience across different phases.

Frequently Asked Questions

1. What is the designation offered by SIRO?

SIRO is hiring for the Senior Regulatory Medical Writer position.

2. How much experience is required?

Candidates must have a minimum of 4 years of relevant regulatory medical writing experience.

3. Is clinical trial experience mandatory?

Yes. Experience across 2–4 phases of clinical trials is mandatory.

4. Are candidates with BA/BE experience eligible?

No. The recruitment announcement specifically states that BA/BE experience will not be considered.

5. Is remote work available?

Yes. Remote working is available for candidates based outside Mumbai. Hybrid working is offered for the Mumbai location.

6. How can candidates apply for this position?

Candidates can email their updated CV to vedanshi.hemani@siroclinpharm.com.

Job Summary

Category	Details
Company	SIRO
Vacancies	Senior Regulatory Medical Writer
Required Education	Not specified in the recruitment announcement
Experience	Minimum 4 years; clinical trial experience across 2–4 phases is mandatory