Author: Sudheer vanguri

BDR Pharmaceuticals International Pvt. Ltd. is conducting a walk-in drive for multiple positions across Analytical Method Validation/Development, Process Engineering, Quality Control, Micro QC, R&D, and Human Resources.
The openings are available across OSD and API divisions, with positions ranging from Apprentice and Officer to Executive, Sr. Executive, and Assistant Manager.
Candidates with qualifications including B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, B.E. Chemical, and M.Sc Organic Chemistry can apply for the relevant positions.
The walk-in interview is scheduled for 3 October 2026, from 10:00 AM to 04:00 PM, at BDR Pharmaceuticals International Private Limited, Luna, Padra, Vadodara.

BDR Pharmaceuticals Analytical Method Validation / Development: OSD Division

HPLC Analyst / Query Response – Officer to Executive

Job Description

• HPLC | Analyst, Query Response | Officer to Executive

Candidates with relevant HPLC analytical and query response experience can apply.

HPLC Reviewer / GC / Query Response – Sr. Executive to Assistant Manager

Job Description

• Reviewer | HPLC, GC, Query Response | Sr. Executive to Asst. Manager

Candidates with relevant experience in HPLC, GC review, and query response activities can apply.

LCMS / GCMS User Analyst – Officer to Executive

Job Description

• User Analyst | LCMS, GCMS | Officer to Executive

Candidates with relevant LCMS and GCMS analytical experience can apply.

XRD / ICPMS User Analyst – Officer to Sr. Officer

Job Description

• User Analyst | XRD + ICPMS | Officer To Sr. Officer

Candidates with relevant experience in XRD and ICPMS analytical activities can apply.

LCMS / ICPMS Reviewer – Executive to Assistant Manager

Job Description

• Reviewer | XRD, LCMS, ICPMS, GCMS | Executive To Assistant Manager

Candidates with relevant analytical review experience can apply.

QA / AMV / AMT / Compliance / Documentation – Officer to Executive

Job Description

• QA | AMV, AMT, Compliance, Documentation | Officer To Executive

Candidates with relevant experience in analytical method validation, analytical method transfer, compliance, and documentation can apply.

Eligibility & Qualifications

The recruitment notification does not specify a single qualification for the Analytical Method Validation / Development positions. Candidates should possess the relevant educational qualification and experience applicable to the respective analytical role.

Relevant qualifications may include: B.Sc | M.Sc | B.Pharm | M.Pharm

BDR Pharmaceuticals Process Engineering / Tech Transfer: API Division

Sr. Officer to Executive

Position Details

• Department: Process Engineering / Tech Transfer
• Division: API
• Position: Sr. Officer to Executive
• Experience: 3–5 Years
• Qualification: B.Tech / B.E. (Chemical)
• Job Function: Process Engineering / Tech Transfer

Eligibility & Qualifications

B.Tech Chemical | B.E. Chemical

Candidates with 3–5 years of relevant experience in process engineering or technology transfer can apply.

BDR Pharmaceuticals Quality Control: OSD Division

Officer to Sr. Executive – HPLC

Position Details

• Department: Quality Control
• Division: OSD
• Position: Officer to Sr. Executive
• Job Role: HPLC
• Additional Opportunity: Apprentice
• Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm

Eligibility & Qualifications

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

Candidates with relevant HPLC and Quality Control experience can apply.

BDR Pharmaceuticals Micro QC: API / OSD Division

Apprentice to Sr. Officer

Position Details

• Department: Micro QC
• Division: API / OSD
• Position: Apprentice to Sr. Officer
• Qualification: B.Sc, M.Sc, Microbiology

Eligibility & Qualifications

B.Sc | M.Sc | B.Sc Microbiology | M.Sc Microbiology

Candidates with relevant Microbiology qualifications and experience can apply.

BDR Pharmaceuticals R&D: API Division

Officer

Position Details

• Department: R&D
• Division: API
• Position: Officer
• Experience: 2–5 Years
• Qualification: M.Sc. (Organic Chemistry)
• Key Skills: Polymorphism, Peptide, LCMS & Synthesis

Eligibility & Qualifications

M.Sc Organic Chemistry

Candidates with relevant R&D experience in polymorphism, peptide, LCMS, and synthesis can apply.

BDR Pharmaceuticals Human Resources: Talent Acquisition

Talent Acquisition Specialist

Position Details

• Department: Human Resources
• Division: Talent Acquisition
• Position: Talent Acquisition Specialist
• Experience: 2–3 Years
• Preference: Pharmaceutical Hiring Exposure Preferred

Eligibility & Qualifications

Candidates with relevant experience in Talent Acquisition and pharmaceutical recruitment can apply.

BDR Pharmaceuticals Recruitment: Key Eligibility

The recruitment covers multiple functions across API and OSD divisions, including analytical development, process engineering, quality control, microbiology, R&D, and talent acquisition.

Eligible Qualifications

B.Sc | M.Sc | B.Pharm | M.Pharm | B.Tech Chemical | B.E. Chemical | M.Sc Organic Chemistry | Microbiology

BDR Pharmaceuticals Walk-In Interview Details

Walk-In Date & Time

Date: 3 October 2026
Time: 10:00 AM to 04:00 PM

Walk-In Venue

BDR Pharmaceuticals International Private Limited
Luna, Padra,
Vadodara, Gujarat

Work Location

BDR Pharmaceuticals International Private Limited
578 & 579, Near Efluent Channel Road,
Village: Luna, Tal. Padra,
Dist. Vadodara – 391440

BDR Pharmaceuticals Contact Details

API Division

Contact Person: Kush Dave (API)
Email: kush.dave@bdrpharma.com

Contact Person: Vidhi Machhi (API)
Email: vidhi.machhi@bdrpharma.com

OSD Division

Contact Person: Pritam Singha (OSD)
Email: pritam.singha@bdrpharma.com

How to Apply

Interested and eligible candidates can attend the walk-in interview on 3 October 2026 between 10:00 AM and 04:00 PM at the BDR Pharmaceuticals facility in Luna, Padra, Vadodara.

The recruitment notification states that the walk-in drive is only for the mentioned opening. Candidates should check the BDR career page for other available roles.

BDR Pharmaceuticals Career Page

Candidates should carry the documents required for the interview and apply for the position relevant to their qualification and experience.

Job Summary

Medpace Clinical Line Manager – CRA, Navi Mumbai

Medpace is hiring a Clinical Line Manager – CRA to lead its Clinical Monitoring team in Navi Mumbai, India.
The position involves leading and line-managing Clinical Research Associates (CRAs), including recruitment, training, coaching, development and resource allocation.
Candidates should have a Bachelor’s degree or higher in Life Sciences or a related discipline, along with clinical monitoring or line-management experience.
The role also requires strong leadership and mentoring skills, advanced knowledge of Good Clinical Practice (GCP) and approximately 10% travel for onsite CRA evaluations.

Medpace Clinical Line Manager – CRA

Job Details

• Company: Medpace
• Position: Clinical Line Manager – CRA
• Job ID: 12173
• Department: Clinical Monitoring
• Location: Navi Mumbai, India
• Employment Type: Full Time
• Travel: Approximately 10%

Clinical Monitoring Leadership

Team Management

The Clinical Line Manager – CRA will be responsible for:

• Leading and line-managing a team of Clinical Research Associates (CRAs).
• Recruiting, training and developing CRAs.
• Providing initial and ongoing training.
• Overseeing and guiding CRAs to ensure they meet expectations for core monitoring responsibilities.
• Conducting regular one-to-one coaching sessions.
• Providing constructive feedback to team members.

CRA Resource Management

• Track and manage CRA resourcing.
• Manage allocation of assignments.
• Support CRA retention and engagement.
• Work toward meeting company objectives related to the Clinical Monitoring team.

Cross-Functional Collaboration

• Collaborate with other functions.
• Work with regional and local operations.
• Work closely with the Senior Director of Clinical Monitoring.

Eligibility & Qualifications

Educational Qualification

• Bachelor’s degree or higher in Life Sciences or a related discipline

Experience

Candidates should meet one of the experience profiles described by Medpace:

• 1–2 years of line-management experience

OR

• An experienced CRA with at least 4 years of clinical monitoring experience who is looking to progress into line management.

Preferred Experience

• Experience working in a global CRO is preferred.
• Advanced knowledge of Good Clinical Practice (GCP).

Key Skills & Competencies

Candidates should demonstrate:

• Strong leadership skills
• Mentoring ability
• Motivational skills
• Effective written communication
• Effective verbal communication
• People-management capabilities
• Coaching and feedback skills
• Ability to manage CRA resources and assignments
• Ability to collaborate with regional and local operations

Eligible Qualification Courses

B.Sc. Life Sciences | M.Sc. Life Sciences | B.Pharm | M.Pharm | Pharm.D | Other relevant Life Science degrees

The source specifies a Bachelor’s degree or higher in Life Sciences or a related discipline; it does not provide a specific course-wise list.

Travel Requirement

The position requires approximately 10% travel for onsite evaluation of CRAs.

Job Location

Navi Mumbai, Maharashtra, India

The position is part of Medpace’s Clinical Monitoring function.

How to Apply

Interested and eligible candidates can apply through the official Medpace careers portal:

Apply for Clinical Line Manager – CRA at Medpace

Job ID: 12173

Job Summary

Labcorp Hiring – Associate for External Application

Labcorp is hiring an Associate for External Application for its Customer Support/Call Centers team in Bengaluru, Karnataka.
The role is based at the Yashwantpur office and involves user access management, application support, troubleshooting and coordination with internal and external users.
Candidates with a Master’s degree in Life Sciences can apply, while knowledge of applications support, project management and customer service is preferred.
This is a full-time, office-based position with rotational shifts, including morning, afternoon and night schedules.

Labcorp Associate for External Application

Job Details

• Company: Labcorp
• Position: Associate for External Application
• Job ID: 2631266
• Category: Customer Support / Call Centers
• Job Type: Full-Time
• Location: Bengaluru, India
• Office: Yashwantpur
• Work Mode: Office-based
• Remote: No

Work Schedule

The position involves rotational shifts:

• 9:00 AM – 6:00 PM
• 2:00 PM – 11:00 PM
• 9:00 PM – 6:00 AM

Job Responsibilities

User Access & Application Support

• Review User Access Request Forms received from clients and internal teams for accuracy.
• Submit User Access Requests in IT Central.
• Follow applicable departmental Standard Operating Procedures (SOPs) and Work Instructions (WIs).
• Act as the first point of contact for internal and external clients.
• Perform troubleshooting to resolve issues in a timely manner.
• Support user access management and application-related processes.

Quality, Productivity & Compliance

• Manage day-to-day tasks while maintaining quality and productivity.
• Complete required training within the specified timelines.
• Ensure timely escalation and issue resolution.
• Ensure regulatory requirements and corporate policies are followed.
• Deliver consistent, high-quality work.

Communication & Stakeholder Coordination

• Build and maintain relationships with internal and external user communities.
• Liaise with internal collaborators for routing and escalation when required.
• Communicate through email, phone and virtual meetings.
• Answer user queries, provide support and escalate issues when necessary.

Research & Problem Solving

• Gather, investigate and research background materials to understand subject matters and systems.
• Use available knowledge bases and understanding of applications, user access management and internal processes to complete tasks.
• Handle multiple tasks in a timely and professional manner.

Eligibility & Qualifications

Minimum Qualification

• Master’s degree in Life Sciences

Preferred Qualifications

• Knowledge of Applications Support
• Knowledge of Project Management
• Customer Service experience
• Local language proficiency in addition to English

Eligible Qualification Courses

M.Sc. Life Sciences | M.Pharm | Pharm.D | M.Sc. Biotechnology | M.Sc. Microbiology | M.Sc. Biochemistry | Other relevant Master’s-level Life Science programs

The official posting specifically states a Master’s degree in Life Sciences as the minimum qualification; the course list above reflects relevant programs within that field.

Skills Required

Microsoft Office Skills

Candidates should have experience and expertise with:

• Microsoft Outlook
• Microsoft Excel
• Microsoft Teams
• Microsoft PowerPoint
• Microsoft Edge
• Microsoft OneNote

Professional Skills

• Problem-solving ability
• Planning and prioritization
• Organization and communication
• Attention to detail
• Strong interpersonal skills
• Ability to work effectively with others
• Ability to manage multiple tasks
• Ability to work under demanding conditions
• Ability to maintain consistent quality and productivity

Location & Work Environment

Job Location: Bengaluru, Karnataka, India

Office Location: Yashwantpur

Work Mode: Office-based

Shift: Rotational

The role requires employees to work from the office and be available for the specified rotational schedules.

How to Apply

Interested and eligible candidates can apply online through the official Labcorp careers portal.

Apply for Associate for External Application – Labcorp

Job ID: 2631266

Job Summary

Clinical Research Coordinator, Dental – Colgate-Palmolive

Colgate-Palmolive is hiring a Clinical Research Coordinator, Dental (Third-Party Payroll) for its R&D operations in Mumbai, Maharashtra.
The role is focused on coordinating oral care clinical trials, participant management, clinical data integrity, regulatory compliance and audit readiness.
Candidates with a BDS degree and 1–2 years of active clinical dental practice are eligible for this opportunity.
The position offers exposure to clinical research, global R&D collaboration, Good Clinical Practice (GCP), clinical trial methodologies and cross-functional operations.

Colgate-Palmolive Clinical Research Coordinator – Dental

Job Details

• Company: Colgate-Palmolive Company
• Position: Clinical Research Coordinator, Dental (Third-Party Payroll)
• Job Number: 176382
• Department: Research & Development
• Location: Mumbai, Maharashtra, India
• Work Mode: On-site
• Employment Type: Full Time
• Payroll: Third-Party Payroll
• Travel: Up to 10%
• Posting Start Date: 27 September 2026
• Relocation Assistance: Not offered

Clinical Research Coordinator – Study Execution & Clinical Operations

The Clinical Research Coordinator will support the end-to-end execution and daily management of internal and external clinical studies related to oral care.

Participant Recruitment & Screening

• Identify, screen and enroll eligible study participants according to protocol criteria.
• Facilitate the informed consent process under Principal Investigator supervision.
• Ensure participants are properly informed and documentation is accurately completed.
• Monitor study subjects and record adverse events (AEs) or protocol deviations.
• Report safety events and protocol deviations promptly.

Investigational Product Handling

• Manage clinical test products.
• Ensure secure storage and accountability of clinical test products.
• Support proper dispensation of investigational or clinical test products.

Data Integrity & Quality Assurance

Clinical Data Management

• Maintain accuracy and integrity of clinical trial data.
• Perform electronic data entry using CRFs/EDC.
• Support clinical data management activities.
• Assist in compiling clinical trial data and organizing study documentation.

Scientific Reporting

• Support preparation of clinical trial reports and presentations.
• Populate Case Report Forms (CRFs/EDC).
• Maintain study-related documentation according to applicable requirements.

Operations & Administrative Responsibilities

Departmental Administration

The Clinical Research Coordinator will support day-to-day administrative and financial operations, including:

• Raising and tracking Purchase Order requests.
• Verifying study invoices against payment milestones.
• Supporting operational budget tracking.
• Assisting with Clinical Trial Agreements (CTAs).
• Supporting processing and execution of service contracts and Non-Disclosure Agreements (NDAs).
• Coordinating with internal teams for study-related agreements and documentation.

Vendor & Supplier Coordination

• Serve as a primary liaison for third-party vendors and suppliers.
• Coordinate timely delivery of research services and clinical supplies.
• Support vendor-related activities associated with clinical research operations.

Facility Maintenance & Audit Readiness

Facility and Equipment Management

• Ensure clinical facilities and testing equipment remain operational.
• Ensure workspaces are properly maintained.
• Support calibration and maintenance of testing equipment according to SOPs.

Audit & Site Compliance

• Maintain continuous inspection and audit readiness.
• Follow Quality & Safety standards.
• Ensure compliance with Good Clinical Practice (GCP) and corporate policies.

Regulatory Compliance & Clinical Research

Regulatory and GCP Activities

• Maintain Trial Master Files (TMF).
• Coordinate submissions and approvals with Institutional Ethics Committees (IEC/IRB).
• Follow applicable regulatory and ethical requirements.
• Support compliance throughout the clinical trial lifecycle.

Cross-Functional Collaboration

• Work within a multidisciplinary team.
• Collaborate with cross-functional R&D and business units.
• Coordinate effectively with internal teams, external vendors and other stakeholders.

Eligibility & Qualifications

Educational Qualification

• Bachelor’s Degree in Dentistry (BDS) from a recognized institution.

Clinical Experience

• 1–2 years of post-degree experience in active clinical dental practice.

Research Background

Prior exposure to any of the following is a strong advantage:

• Dental research
• Clinical trials
• Basic research
• Academic research projects

Regulatory & Quality Knowledge

Candidates should have knowledge of:

• Regulatory requirements
• Ethical guidelines
• IEC/IRB requirements
• Good Clinical Practice (GCP) standards

Skills & Competencies

• Strong organizational skills
• Clinical research coordination
• Excellent written and verbal communication
• Presentation skills
• Ability to work in a multidisciplinary environment
• Ability to manage departmental administration
• Facility maintenance and audit-readiness activities
• Attention to detail
• Ability to work with electronic data management systems
• Familiarity with relevant software suites
• Flexibility to meet clinical trial requirements
• Willingness to travel up to 10%

Eligible Qualification Courses

BDS | Bachelor of Dental Surgery

Career Growth & Learning Opportunities

The role provides exposure to:

• Corporate R&D and global technology integration
• Clinical trial execution
• Clinical research operations
• Site management
• Facility maintenance
• Clinical data integrity
• Quality and Safety systems
• Audit-ready research environments
• Global R&D collaboration
• Technical and professional mentorship

Location & Work Environment

Job Location: Mumbai, Maharashtra, India

Work Mode: On-site

Travel Requirement: Up to 10% of working time.

The position requires flexibility in working hours according to clinical trial requirements.

How to Apply

Interested and eligible candidates can apply through the official Colgate-Palmolive careers portal:

Apply for Clinical Research Coordinator, Dental – Colgate-Palmolive

Job Number: 176382

Job Summary

Naprod Life Sciences Pvt. Ltd. is conducting a walk-in interview for multiple positions across Microbiology, Quality Control, Quality Assurance, F&D (Injectable), and Engineering.
The openings include App/Trainee, Officer, Executive, and Officer-HVAC positions for freshers and experienced pharmaceutical professionals.
Candidates with qualifications including B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma, and B.E./B.Tech can apply for the respective roles.
The recruitment is specifically seeking candidates with experience in pharmaceutical companies, particularly formulation injectable manufacturing, with male candidates specified for most positions.

Naprod Life Sciences Microbiology Department: App/Trainee

Position Details

• Designation: App/Trainee
• Experience: Fresher
• Qualification: B.Sc / M.Sc (Micro / Biotech)
• Openings: 6
• Gender: Male
• Job Role: Basic Knowledge of Microbiology

Eligibility & Qualifications

B.Sc Microbiology | M.Sc Microbiology | B.Sc Biotechnology | M.Sc Biotechnology

Freshers with a relevant Microbiology or Biotechnology qualification and basic knowledge of microbiology can apply.

Naprod Life Sciences Microbiology Department: Officer

Position Details

• Designation: Officer
• Experience: 1–3 Years
• Qualification: B.Sc / M.Sc (Micro / Biotech)
• Openings: 5
• Gender: Male
• Job Role: Experience in Environmental Monitoring

Eligibility & Qualifications

B.Sc Microbiology | M.Sc Microbiology | B.Sc Biotechnology | M.Sc Biotechnology

Candidates with relevant pharmaceutical microbiology experience and practical experience in environmental monitoring can apply.

Naprod Life Sciences Quality Control Department: Officer

Position Details

• Designation: Officer
• Experience: 2–5 Years
• Qualification: B.Sc / M.Sc (Chemistry)
• Openings: 3
• Gender: Male
• Job Role: Experience in Finished Section, HPLC Handled

Eligibility & Qualifications

B.Sc Chemistry | M.Sc Chemistry

Candidates with relevant Quality Control experience in the finished product section and hands-on HPLC experience can apply.

Naprod Life Sciences Quality Assurance Department: Executive

Position Details

• Designation: Executive
• Experience: 4–6 Years
• Qualification: B.Pharm / M.Pharm
• Openings: 1
• Gender: Male
• Job Role: IPQA Activity

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with relevant experience in IPQA activities within pharmaceutical manufacturing can apply.

Naprod Life Sciences Quality Assurance Department: Officer

Position Details

• Designation: Officer
• Experience: 2–4 Years
• Qualification: B.Pharm / M.Pharm
• Openings: 1
• Gender: Male / Female
• Job Role: APQR Preparation

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with relevant experience in Annual Product Quality Review (APQR) preparation can apply.

Naprod Life Sciences F&D Injectable Department: Executive

Position Details

• Designation: Executive
• Experience: 4–6 Years
• Qualification: B.Pharm / M.Pharm
• Openings: 1
• Gender: Male
• Job Role: PV Batches, Literature Search, Patent Review, MFR & PDR

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with relevant formulation and development experience involving PV batches, literature search, patent review, MFR, and PDR activities can apply.

Naprod Life Sciences Engineering Department: Officer – HVAC

Position Details

• Designation: Officer – HVAC
• Experience: 2–4 Years
• Qualification: Diploma / B.E. / B.Tech
• Openings: 1
• Gender: Male
• Job Role: HVAC Maintenance, Area Validation, Particle Count

Eligibility & Qualifications

Diploma | B.E. | B.Tech

Candidates with relevant HVAC experience in pharmaceutical manufacturing, including HVAC maintenance, area validation, and particle count activities, can apply.

Naprod Life Sciences Recruitment: Eligibility & Experience

The recruitment includes opportunities for both freshers and experienced professionals across different departments.

Experience Requirements

• Microbiology App/Trainee: Fresher
• Microbiology Officer: 1–3 Years
• QC Officer: 2–5 Years
• QA Executive: 4–6 Years
• QA Officer: 2–4 Years
• F&D Executive: 4–6 Years
• Engineering Officer – HVAC: 2–4 Years

Eligible Qualifications

B.Sc | M.Sc | B.Pharm | M.Pharm | Diploma | B.E. | B.Tech | Microbiology | Biotechnology | Chemistry

Naprod Life Sciences Walk-In Interview Details

Walk-In Date & Time

Date: 28 September to 01 October 2026
Time: 10:00 AM to 04:00 PM

Walk-In Venue

Naprod Life Sciences Pvt. Ltd. – Boisar
Plot No. G-17/1, MIDC Boisar,
Dist. Palghar, Maharashtra

Important Experience Requirement

Experience must be in a pharmaceutical company, specifically Formulation Injectable.

The recruitment notification also specifies male candidates for most positions, while the QA Officer position is listed for Male / Female candidates.

Documents Required for Naprod Life Sciences Walk-In Interview

Candidates should bring the following documents:

• Updated CV
• Last 3 months’ salary slips
• Current company appointment letter
• Increment letter
• Aadhaar Card
• PAN Card
• Qualification marksheet
• Passport-size photograph

How to Apply

Interested and eligible candidates can attend the walk-in interview at the Naprod Life Sciences facility in Boisar between 28 September and 01 October 2026, from 10:00 AM to 04:00 PM.

Candidates should carry their updated CV and all required documents mentioned in the recruitment notification.

Candidates can also contact the recruitment team for further details.

Email: seema.patel@naprodgroup.com

Contact: 8421403723 / 8087288136 / 7507846468

Job Summary

Apnar Pharma Private Limited, a subsidiary of Senores Pharmaceuticals Limited, is conducting walk-in interviews for multiple positions across QA, QC, Production, Packaging, Warehouse, and Tech Transfer.
The openings are available for professionals with qualifications including B.Pharm, M.Pharm, M.Sc, B.Sc, ITI, and Graduation.
Candidates with relevant pharmaceutical industry experience ranging from 2 to 10 years can apply for the respective positions.
The walk-in interview is scheduled for 04 October 2026, from 10:00 AM to 03:00 PM, in Vadodara, Gujarat.

Assistant Manager / Executive / Sr. Officer

Position Details

• Department: QA
• Position: Asst. Manager / Executive / Sr. Officer
• Key Skills: Vendor qualification, SAP management & Training Management
• Qualification: B.Pharm, M.Pharm, M.Sc.
• Experience: 3–10 Years

Eligibility & Qualifications

B.Pharm | M.Pharm | M.Sc

Candidates with relevant experience in vendor qualification, SAP management, and training management can apply.

Apnar Pharma Quality Assurance Department: Executive / Officer

Position Details

• Department: QA
• Position: Executive / Officer
• Key Skills: Documentation, Validation, Equipment Qualification, IPQA & Stability
• Qualification: B.Pharm, M.Pharm, M.Sc.
• Experience: 3–5 Years

Eligibility & Qualifications

B.Pharm | M.Pharm | M.Sc

Candidates with relevant experience in QA documentation, validation, equipment qualification, IPQA, and stability activities can apply.

Apnar Pharma Quality Assurance Department: Executive / Officer – Analytical QA

Position Details

• Department: QA
• Position: Executive / Officer
• Key Skills: Analytical QA
• Qualification: B.Pharm, M.Pharm, M.Sc.
• Experience: 3–5 Years

Eligibility & Qualifications

B.Pharm | M.Pharm | M.Sc

Candidates with relevant experience in Analytical Quality Assurance can apply.

Apnar Pharma Quality Control Department: Officer / Sr. Officer

Position Details

• Department: QC
• Position: Officer / Sr. Officer
• Key Skills: RM/PM Sampling & Analysis | HPLC/GC Testing | GLP Compliance
• Qualification: B.Sc, M.Sc.
• Experience: 2–4 Years

Eligibility & Qualifications

B.Sc | M.Sc

Candidates with relevant experience in raw material and packing material sampling and analysis, HPLC/GC testing, and GLP compliance can apply.

Apnar Pharma Quality Control Department: Executive / Sr. Executive

Position Details

• Department: QC
• Position: Executive / Sr. Executive
• Key Skills: Documentation + QMS
• Qualification: B.Sc, M.Sc.
• Experience: 4–7 Years

Eligibility & Qualifications

B.Sc | M.Sc

Candidates with relevant experience in QC documentation and Quality Management Systems can apply.

Apnar Pharma Quality Control Department: Sr. Executive

Position Details

• Department: QC
• Position: Sr. Executive
• Key Skills: Reviewer, RM/IP/FP Raw Data & Audit Trail Review
• Qualification: B.Sc, M.Sc.
• Experience: 5–8 Years

Eligibility & Qualifications

B.Sc | M.Sc

Candidates with relevant experience in raw material, in-process, finished product raw data review and audit trail review can apply.

Apnar Pharma Production Department: Supervisor / Executive

Position Details

• Department: Production
• Position: Supervisor / Executive
• Key Skills: Capsule Filling, Compression, Coating & P&E Area, USFDA Compliance
• Qualification: B.Pharm, M.Pharm, M.Sc.
• Experience: 4–7 Years

Eligibility & Qualifications

B.Pharm | M.Pharm | M.Sc

Candidates with relevant pharmaceutical production experience in capsule filling, compression, coating, P&E areas, and USFDA compliance can apply.

Apnar Pharma Production Department: Operator

Position Details

• Department: Production
• Position: Operator
• Key Skills: Coating | Fully Automatic Capsule Filling
• Qualification: ITI
• Experience: 3–7 Years

Eligibility & Qualifications

ITI

Candidates with relevant experience in coating and fully automatic capsule filling operations can apply.

Apnar Pharma Production Packaging Department: Operator

Position Details

• Department: Production – Packaging
• Position: Operator
• Key Skills: Secondary Bottle Packing, CVC Line Machine
• Qualification: ITI
• Experience: 3–7 Years

Eligibility & Qualifications

ITI

Candidates with relevant experience in secondary bottle packing and CVC line machine operations can apply.

Apnar Pharma Warehouse Department: Executive / Sr. Executive

Position Details

• Department: Warehouse
• Position: Executive / Sr. Executive
• Key Skills: Warehouse Management, Stock Control, Dispensing & Dispatch
• Qualification: Graduation
• Experience: 4–8 Years

Eligibility & Qualifications

Any Graduation

Candidates with relevant experience in warehouse management, stock control, dispensing, and dispatch activities can apply.

Apnar Pharma Tech Transfer Department: Assistant Manager & Sr. Executive

Position Details

• Department: Tech Transfer
• Position: Asst. Manager & Sr. Executive
• Key Skills: Scale Up & Exhibit Batches, Tech Transfer, Troubleshoot & ANDA Evaluation
• Qualification: B.Pharm, M.Pharm
• Experience: 5–10 Years

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with relevant experience in scale-up, exhibit batches, technology transfer, troubleshooting, and ANDA evaluation can apply.

Apnar Pharma Recruitment: Experience Requirements

The recruitment includes positions requiring 2–10 years of relevant pharmaceutical experience, depending on the role.

Experience Range

• QA: 3–10 Years
• QC: 2–8 Years
• Production: 3–7 Years
• Production – Packaging: 3–7 Years
• Warehouse: 4–8 Years
• Tech Transfer: 5–10 Years

Apnar Pharma Recruitment: Regulated Markets Experience

Experience in regulated markets is preferred.

Candidates with relevant experience in regulated pharmaceutical markets can apply for the respective positions.

Apnar Pharma Walk-In Interview Details

Walk-In Date & Time

Date: 04 October 2026, Sunday
Time: 10:00 AM to 03:00 PM

Walk-In Venue

Ginger RCR
9, Race Course Rd, Near RBL Bank,
Gadapura, Diwalipura, Vadodara, Gujarat

Job Location

Apnar Pharma Private Limited
USFDA & MHRA Approved Formulation Plant

Block No. 102, At & Post Gavasad,
Padra Jambusar Road, Taluka Padra,
District Vadodara – 391430, Gujarat

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue on 04 October 2026, between 10:00 AM and 03:00 PM.

Candidates who are unable to attend the walk-in interview can share their updated resume with the recruitment team.

Email: neel@senorespharma.com

Contact: +91 91066 17844

Candidates should mention the position applied for and highlight their relevant pharmaceutical experience in their resume.

Job Summary

Sycon Clinical Research Pvt. Ltd. is hiring professionals for Junior Analyst – Bioanalytical and Senior Analyst – Bioanalytical positions in Ahmedabad.
The openings are available in the Bioanalytical Department for candidates with relevant laboratory experience.
Candidates with M.Sc, B.Pharm, or M.Pharm qualifications and 2–6 years of bioanalytical laboratory experience can apply.
The roles involve LC-MS/MS analysis, sample preparation, laboratory documentation, and GCP/GLP compliance activities.

Junior Analyst – Bioanalytical

Position Details

• Position: Junior Analyst – Bioanalytical
• Department: Bioanalytical
• Location: Ahmedabad
• Experience: 2–6 Years of relevant experience in a bioanalytical lab
• Salary: No bar for deserving candidate

Key Responsibilities

• Analyze bioanalytical samples such as plasma, serum, urine, whole blood, tissue, etc. using LC-MS/MS.
• Perform sample preparation techniques like PPT, LLE, and SPE.
• Ensure proper documentation and data entry.
• Follow GCP/GLP, safety and compliance requirements.

Eligibility & Qualifications

M.Sc | B.Pharm | M.Pharm

Candidates should have relevant experience in a bioanalytical laboratory and practical exposure to LC-MS/MS instruments.

Senior Analyst – Bioanalytical

Position Details

• Position: Senior Analyst – Bioanalytical
• Department: Bioanalytical
• Location: Ahmedabad
• Experience: 2–6 Years of relevant experience in a bioanalytical lab
• Salary: No bar for deserving candidate

Key Responsibilities

• Analyze bioanalytical samples such as plasma, serum, urine, whole blood, tissue, etc. using LC-MS/MS.
• Perform sample preparation techniques like PPT, LLE, and SPE.
• Ensure proper documentation and data entry.
• Follow GCP/GLP, safety and compliance requirements.

Eligibility & Qualifications

M.Sc | B.Pharm | M.Pharm

Candidates with relevant bioanalytical laboratory experience and hands-on LC-MS/MS experience can apply.

Technical Requirements

LC-MS/MS Experience

Candidates should have 2–6 years of experience in a bioanalytical laboratory with hands-on experience in LC-MS/MS instruments, including systems such as:

• Sciex 4000
• Sciex 4500
• Sciex 5500
• Sciex 6500+
• Waters TQ

Analyst Software Experience

Experience with relevant analyst software is required, including:

• Analyst software (1.4.3 / OS)
• MassLynx
• Mass Connect

Additional Requirements

• Good knowledge of GCP/GLP and laboratory documentation.
• Proficiency in MS Office.
• Practical experience in bioanalytical sample analysis and preparation.

Work Environment

Sycon Clinical Research offers a dynamic CRO setup with high-quality standards and compliance.

The positions are part of the company’s bioanalytical team supporting clinical research activities.

Location & Salary

Location: Ahmedabad

Salary: No bar for deserving candidate.

The recruitment notification does not provide a fixed salary range.

How to Apply

Interested candidates can send their updated resume to the recruitment team.

Email: hr@syconcro.com

Candidates should mention the position applied for and highlight their experience in bioanalytical laboratory operations, LC-MS/MS, sample preparation, and relevant software.

Candidates can also learn more about Sycon Clinical Research through the company’s website mentioned in the recruitment notification.

Job Summary

Softgel Healthcare Pvt. Ltd. is hiring a QMS Executive for its pharmaceutical softgel capsule manufacturing unit.
The position is suitable for professionals with 2 to 5 years of experience in Regulatory Pharmaceutical QMS.
Candidates with B.Pharm, M.Pharm, B.Sc Chemistry, M.Sc Chemistry, or relevant qualifications can apply.
The role involves SOP management, change controls, deviations, quality risk assessments, CAPA, audit compliance, and GMP/QMS activities.

QMS Executive

Position Details

• Position: QMS Executive
• Experience: 2–5 Years
• Required Experience: Only in Regulatory Pharmaceutical QMS
• Industry: Pharmaceutical Softgel Capsule Manufacturing

Key Responsibilities

• Preparation, review and revision of SOPs.
• Handling of Change Control & Deviations.
• Preparation/coordination of Quality Risk Assessments (QRA).
• CAPA management and timely closure.
• Handling Audit Compliance and closure of observations.
• Ensuring compliance with GMP and QMS requirements.

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc Chemistry | M.Sc Chemistry | Relevant Qualification

Candidates should have 2–5 years of experience specifically in Regulatory Pharmaceutical QMS.

Experience Requirements

Required Experience

2–5 Years

The recruitment notification specifically mentions experience only in Regulatory Pharmaceutical QMS.

Candidates with relevant experience in pharmaceutical QMS, regulatory compliance, SOP management, change control, deviations, CAPA, quality risk assessments, and audit compliance can apply.

Key Skills

Quality Management System

The selected candidate will be responsible for activities related to:

• SOP preparation, review and revision
• Change Control
• Deviation Management
• Quality Risk Assessments (QRA)
• CAPA Management
• Audit Compliance
• Closure of Audit Observations
• GMP Compliance
• QMS Requirements

Job Location

The recruitment notification does not mention the job location.

The position is for a Pharmaceutical Softgel Capsule Manufacturing Unit.

How to Apply

Interested and eligible candidates can share their updated resume with the recruitment team through email.

Email: ta@softgelhealthcare.com

Candidates should ensure that their resume clearly highlights their Regulatory Pharmaceutical QMS experience along with their educational qualification and relevant quality management experience.

Job Summary

Verve Human Care Laboratories, a unit of Venor Pharma Ltd., is hiring experienced professionals for multiple positions in its Microbiology Department.
The openings include Sr. Officer / Sr. Executive, Operator – Autoclave, Trainee – Sr. Officer, and Assistant Manager roles.
Candidates with M.Sc Microbiology and relevant pharmaceutical microbiology experience can apply for the respective positions.
The available opportunities require 1–10 years of experience, depending on the designation.

Verve Human Care Laboratories Microbiology Department: Sr. Officer / Sr. Executive

Position Details

• No. of Openings: 1
• Designation: Sr. Officer – Sr. Executive (AMV of MLT, AMV of BET)
• Department: Microbiology
• Qualification: M.Sc Microbiology
• Experience: 3–7 Years

Eligibility & Qualifications

M.Sc Microbiology

Candidates with relevant experience in pharmaceutical microbiology and AMV of MLT and BET activities can apply.

Verve Human Care Laboratories Microbiology Department: Operator – Autoclave

Position Details

• No. of Openings: 1
• Designation: Operator – Autoclave (Regulatory requirement)
• Department: Microbiology
• Qualification: M.Sc Microbiology
• Experience: 3–5 Years

Eligibility & Qualifications

M.Sc Microbiology

Candidates with relevant experience in microbiology operations and autoclave activities can apply for this position.

Verve Human Care Laboratories Microbiology Department: Trainee – Sr. Officer

Position Details

• No. of Openings: 3
• Designation: Trainee – Sr. Officer (Regulatory Compliance)
• Department: Microbiology
• Qualification: M.Sc Microbiology
• Experience: 1–2 Years

Eligibility & Qualifications

M.Sc Microbiology

Candidates with relevant experience in microbiology and regulatory compliance activities can apply.

Verve Human Care Laboratories Microbiology Department: Assistant Manager

Position Details

• No. of Openings: 1
• Designation: Assistant Manager (AMV, HTS, Qualification)
• Department: Microbiology
• Qualification: M.Sc Microbiology
• Experience: 5–10 Years

Eligibility & Qualifications

M.Sc Microbiology

Candidates with relevant experience in AMV, HTS, qualification, and pharmaceutical microbiology activities can apply.

Verve Human Care Laboratories Microbiology Jobs: Experience

The recruitment is open to candidates with relevant experience ranging from 1 to 10 years, depending on the position.

Experience Requirements

• Trainee – Sr. Officer: 1–2 Years
• Sr. Officer – Sr. Executive: 3–7 Years
• Operator – Autoclave: 3–5 Years
• Assistant Manager: 5–10 Years

Verve Human Care Laboratories Microbiology Jobs: Qualification

Eligibility & Qualifications

M.Sc Microbiology

The recruitment notification specifically mentions M.Sc Microbiology as the required qualification for all listed positions.

Verve Human Care Laboratories Microbiology Jobs: Work Location

Work Location:
Plot No. 15A, Pharmacity, Selaqui,
Dehradun, Uttarakhand

How to Apply

Interested and eligible candidates can share their updated resume with the recruitment team.

Email: hr1@vervehumancare.com

For recruitment-related queries, candidates can contact:

Contact Number: 9762988464

Candidates should mention the position applied for clearly in their resume and highlight relevant experience in pharmaceutical microbiology.

Job Summary

Eureka GBA Group is hiring an Analyst – Nutraceutical for its team in Bangalore.
The position is suitable for graduates and post-graduates with a background in Science.
Candidates with a minimum of 1 year of relevant experience can apply for this opportunity.
Interested candidates can share their updated CV with the recruitment team through the email address provided below.

Eureka GBA Group Nutraceutical Department: Analyst

Position Details

• Position: Analyst – Nutraceutical
• Location: Bangalore
• Minimum Experience: 1 Year
• Qualification: Graduate / Post-Graduate in Science

Eligibility & Qualifications

B.Sc | M.Sc | Other Relevant Science Graduates | Relevant Science Post-Graduates

Candidates with a relevant Science background and at least 1 year of experience can apply for the Analyst – Nutraceutical position.

Eureka GBA Group Analyst – Nutraceutical: Experience

Minimum Experience: 1 Year

Candidates should have relevant professional experience applicable to analytical or nutraceutical-related activities.

Eureka GBA Group Analyst – Nutraceutical: Job Location

Location: Bangalore

The selected candidate will be based in Bangalore.

How to Apply

Interested and eligible candidates can share their updated CV with the recruitment team through the email address mentioned in the recruitment notification.

Email: HR@eurekaserv.com

Candidates should ensure that their resume clearly mentions their educational qualification and relevant work experience.

Job Summary