Job Tag: Pharma Jobs in Ahmedabad

Senior Regulatory Affairs Executive Vacancy | Bonetech Medisys

Apply for Senior Regulatory Affairs Executive role at Bonetech Medisys Pvt. Ltd. Full-time position with global regulatory compliance responsibilities.

Bonetech Medisys Pvt. Ltd., a trusted name in the medical devices industry, is inviting applications for the role of Senior Regulatory Affairs Executive. This is a full-time opportunity for professionals seeking to build a career in global regulatory compliance, ensuring products meet international standards and safety requirements. If you have experience with EU MDR, FDA 510(k), ISO 14971, and IEC 62366-1, this role provides an excellent platform to showcase your expertise.

Company Overview

Bonetech Medisys Pvt. Ltd. is a leading healthcare and medical devices company committed to innovation, quality, and global compliance. With a strong focus on developing advanced orthopedic and surgical solutions, Bonetech Medisys works with international regulatory frameworks to bring safe and effective products to market. The company emphasizes quality assurance, patient safety, and continuous improvement, making it a reliable name in the industry.

Job Role & Responsibilities

As a Senior Regulatory Affairs Executive, you will play a critical role in ensuring that Bonetech’s products comply with global regulatory requirements. Your responsibilities will include:

• Preparing and updating regulatory submissions in line with EU MDR and FDA 510(k) requirements.
• Developing and maintaining risk management documentation as per ISO 14971 and usability engineering under IEC 62366-1.
• Reviewing and approving product labeling, IFUs (Instructions for Use), surgical technique guides, and promotional materials for regulatory compliance.
• Developing and updating SOPs to align with evolving regulatory requirements.
• Leading and compiling documentation for product registrations, license renewals, and market approvals.
• Monitoring global regulatory changes and ensuring timely compliance updates.
• Acting as a regulatory representative in new product development (NPD) teams, advising on global compliance strategies.
• Liaising with Notified Bodies, FDA, distributors, and suppliers on regulatory matters.
• Supporting and leading external audits/inspections, coordinating with auditors.
• Providing regulatory training to cross-functional teams and maintaining awareness of quality system requirements.
• Monitoring vigilance databases for adverse events and recall trends.

Eligibility / Qualifications

• Education: B. Pharm, M. Pharm, M.Sc (Life Sciences), Biomedical Engineering, or equivalent degree.
• Experience: 3–7 years in Regulatory Affairs (Medical Devices/Pharma preferred).
• Certifications: Knowledge of EU MDR, FDA 510(k), ISO 13485, ISO 14971, IEC 62366-1.
• Skills Required: Strong understanding of global regulatory processes, excellent communication skills, and ability to manage audits and submissions.

Location & Salary

• Job Type: Full-time
• Location: India (Company HQ: Bonetech Medisys Pvt. Ltd.)
• Salary: Competitive, based on qualifications and experience.

Application Process

Interested candidates can apply by sending their updated resume to:

• Email: hr@bonetechmedisys.com
• Phone: +91 95128 57704
• Website: www.bonetechmedisys.com

FAQs

1. Who can apply for the Senior Regulatory Affairs Executive role?
Candidates with a background in pharmacy, life sciences, or biomedical engineering, along with regulatory experience in EU MDR and FDA compliance, are eligible.

2. Is prior experience mandatory?
Yes, candidates should have 3–7 years of experience in regulatory affairs, preferably in medical devices or pharma.

3. What certifications are required?
Hands-on knowledge of EU MDR, FDA 510(k), ISO 13485, ISO 14971, IEC 62366-1 is required.

4. What is the salary range for this role?
Salary is competitive and based on candidate’s experience and expertise.

5. What is the scope of this role?
This role involves global regulatory compliance, audits, risk management, labeling, and acting as a regulatory point of contact with authorities.

Apply before 23rd August 2025 to secure your place in Bonetech’s regulatory team!

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AcuLIFE Hiring QC Chemists/Executives | 2+ Yrs Exp Required

Apply for Quality Control Chemist/Executive roles at AcuLIFE. Pharma & science graduates with 2+ years’ QC/ADL experience in pharma/injectables.

AcuLIFE Healthcare, a trusted name in pharmaceuticals for over 30 years, is inviting applications for Chemist/Executive positions in Quality Control (QC) and Analytical Development Laboratory (ADL). This opportunity is ideal for professionals with 2+ years of experience in pharmaceutical quality control, especially in injectables.

Company Overview

AcuLIFE has been prescribing healthcare innovation for more than three decades, with a strong reputation in the pharmaceutical and healthcare industry. The company specializes in injectables and other life-saving products, following stringent regulatory compliance, global quality standards, and advanced QC practices. A career at AcuLIFE provides exposure to cutting-edge technology and the chance to contribute to global healthcare.

Job Role & Responsibilities

Chemist / Executive – Quality Control (QC) / ADL

• Experience: Minimum 2 Years in QC/ADL (preferably in pharmaceutical/injectable sector)
• Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm

Key Responsibilities:

• Conduct testing and analysis of raw materials, in-process samples, and finished injectable products.
• Support analytical method validation and qualification of laboratory instruments.
• Ensure regulatory compliance with pharmacopoeia standards and quality control processes.
• Operate and maintain instruments like HPLC, GC, and UV-Vis spectrophotometers.
• Prepare accurate and complete documentation of experimental data.

Eligibility / Qualifications

• Education: Science and Pharmacy graduates – B.Sc, M.Sc, B.Pharm, M.Pharm.
• Experience: 2–3+ years in QC/ADL.
• Preferred Background: Pharma manufacturing or injectable sector.

Relevant courses: B.Sc Chemistry, M.Sc Chemistry, B.Pharm (Pharmaceutical Sciences), M.Pharm (Pharmaceutical Analysis, Quality Assurance, Pharmaceutics).

Location & Salary

• Work Location: AcuLIFE Healthcare facilities (exact location details to be shared during recruitment).
• Salary: Competitive salary package as per industry standards with benefits and career advancement opportunities.

Application Process

Interested candidates can apply by sending their updated CVs to the HR department:

Email Contacts:

• recruitment@aculife.co.in
• rajeshthakor@aculife.co.in

Apply today to secure your position with a company that has been driving pharmaceutical innovation for 30+ years.

FAQs

1. Who can apply for the QC Chemist/Executive role?
Science and pharmacy graduates with at least 2 years of QC/ADL experience.

2. Is injectable sector experience required?
Preferred, but not mandatory. Experience in pharma QC is essential.

3. What instruments should candidates know?
HPLC, GC, and UV-Vis spectrophotometers.

4. What are the main responsibilities?
Testing, analysis, method validation, equipment handling, and regulatory compliance.

5. How to apply?
Email your resume to recruitment@aculife.co.in or rajeshthakor@aculife.co.in.

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HOF Pharma Hiring QC Officers & Executives | Ahmedabad

Apply for QC Officer & QC Executive positions at HOF Pharmaceuticals, Ahmedabad. Pharma graduates with 1–4 yrs formulation experience required.

HOF Pharmaceuticals Limited, a WHO-GMP certified pharmaceutical manufacturing company, is inviting applications for Quality Control (QC) Officer and QC Executive positions at its facility in Sanand, Ahmedabad. This opportunity is ideal for pharma professionals with 1–4 years of formulation (OSD) experience who want to grow their career with a trusted pharmaceutical brand.

Company Overview

HOF Pharmaceuticals is a reputed pharmaceutical company, committed to manufacturing high-quality formulations while maintaining compliance with WHO-GMP and global regulatory standards. The company emphasizes innovation, robust quality systems, and employee growth. Joining HOF Pharma provides exposure to advanced QC operations, modern analytical techniques, and a professional work culture.

Job Role & Responsibilities

QC Officer / QC Executive

• Experience: 1–4 Years (in Pharma Formulations – OSD)
• Qualification: B.Pharm, M.Pharm, M.Sc
• Key Responsibilities:
  • Conduct routine analysis of raw materials, finished products, and stability samples.
  • Operate analytical instruments like HPLC, UV, IR, and others.
  • Handle in-process and finished product testing and sampling.
  • Maintain documentation in compliance with WHO-GMP and regulatory standards.
  • Support audits, validations, and compliance activities.

Eligibility / Qualifications

• Required Education: B.Pharm, M.Pharm, M.Sc (Analytical Chemistry, Pharmaceutical Analysis, Quality Assurance).
• Experience: 1–4 years in Quality Control within formulation (OSD) units.
• Skills Required:
  • Strong knowledge of cGMP and quality systems.
  • Hands-on expertise in analytical techniques and instrument operations.
  • Effective documentation and communication skills.

Location & Salary

• Job Location: HOF Pharmaceuticals Ltd., Sanand, Ahmedabad, Gujarat.
• Salary: Competitive salary package with benefits, based on qualifications and experience.

Application Process

Interested candidates can send their updated resumes directly to the company’s HR department:

Email: hr@hofpharma.com

Apply before 23rd August 2025 to secure your opportunity with a WHO-GMP certified pharma manufacturer.

FAQs

1. Who can apply for these QC positions?
Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and 1–4 years’ QC experience in pharma formulations (OSD).

2. What instruments should candidates be familiar with?
HPLC, UV, IR, and other analytical tools used in pharmaceutical QC.

3. Is prior pharma experience mandatory?
Yes, candidates should have 1–4 years of experience in pharma formulations QC.

4. Where is the job location?
Sanand, Ahmedabad, Gujarat.

5. How to apply?
Send your CV to hr@hofpharma.com.

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Swiss Parenterals Ltd – Officer/Executive QA Production QMS Vacancies in Ahmedabad

Apply for Officer to Executive roles in Production QMS at Swiss Parenterals Ltd, Ahmedabad. Openings for B.Pharm, M.Pharm, B.Sc, M.Sc with 1–5 years of experience.

Swiss Parenterals Ltd. is inviting talented professionals to join its Production QMS (Injectable) team in Ahmedabad. This walk-in drive is an excellent opportunity for pharma professionals with experience in Quality Management Systems, injectable production, and regulatory compliance. If you are looking for career growth in the pharmaceutical industry with a trusted name, this is your chance.

Company Overview

Swiss Parenterals Ltd. is a reputed pharmaceutical company recognized for its advanced manufacturing of injectable formulations. With state-of-the-art facilities and a strong focus on quality assurance, global regulatory standards, and innovation, Swiss Parenterals continues to be a key player in providing high-quality parenteral solutions worldwide. Joining Swiss Parenterals means being part of a company committed to patient safety and pharmaceutical excellence.

Job Role & Responsibilities

The openings are for Officer to Executive positions in Production QMS (Injectables). Selected candidates will be responsible for:

• Managing and executing Change Control activities.
• Handling Deviation Reports to ensure compliance.
• Investigating and addressing Market Complaints.
• Monitoring and resolving OOS (Out of Specification) and OOT (Out of Trend) issues.
• Implementing CAPA (Corrective and Preventive Actions) effectively.
• Supporting documentation, SOP adherence, and audit preparedness.

This role requires hands-on experience in pharmaceutical QMS, ensuring compliance with GMP guidelines and global regulatory expectations.

Eligibility / Qualifications

Candidates should meet the following criteria:

• Qualification: B.Pharm, M.Pharm, B.Sc, or M.Sc.
• Experience: 1 to 5 years in QMS/Production (Injectable segment preferred).
• Strong knowledge of CAPA, OOS/OOT handling, and Change Control management.
• Experience in handling regulatory audits and ensuring GMP compliance is an added advantage.

Relevant education includes:

• B.Pharm, M.Pharm, B.Sc (Chemistry, Biotechnology, Microbiology), M.Sc (Pharmaceutical Sciences, Chemistry, Biotechnology).

Location & Salary

• Work Location: Swiss Parenterals Ltd., Unit I: 808, 809, 810, Kerala Industrial Estate, GIDC, Bavla, Ahmedabad – 382220.
• Salary will be commensurate with qualifications, experience, and industry standards.

Application Process

This is a Walk-In Interview opportunity:

• Date: Saturday, 23rd August 2025
• Time: 09:00 AM to 02:00 PM
• Venue: Swiss Parenterals Ltd., Unit I, Bavla, Ahmedabad
• Documents Required: Updated Resume, Last 3 Months’ Salary Slips, Recent Passport-Size Photograph
• Contact Numbers: +91 63529 78952 / +91 99789 76432
• Email IDs for CV Submission: recruitment@swiss.in, hr1@swiss.in

Applicants unable to attend the walk-in can still apply via email. Apply before the interview date to secure your spot!

FAQs

1. Who can apply for Swiss Parenterals Production QMS vacancies?
Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc and 1–5 years of experience in Production QMS or Injectables can apply.

2. What is the interview date for Swiss Parenterals jobs in Ahmedabad?
The walk-in interview will be held on 23rd August 2025 (Saturday) from 09:00 AM to 02:00 PM.

3. Is prior injectable manufacturing experience necessary?
Yes, candidates with injectable production/QMS experience will be preferred, though relevant QMS backgrounds may also be considered.

4. Can freshers apply for Swiss Parenterals Ltd vacancies?
No, these openings require 1–5 years of relevant industry experience.

5. How can I apply if I cannot attend the walk-in?
You can email your updated resume to recruitment@swiss.in or hr1@swiss.in.

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QA Officer Vacancies | B.Pharm/M.Pharm with 2–4 Years Experience | S Kant Healthcare

Apply at S Kant Healthcare for QA Officer (QMS) openings. Open for B.Pharm/M.Pharm graduates with 2–4 years of experience in APQR, change control & deviation.

Looking for a career in Quality Assurance (QA) with a reputed pharmaceutical organization? S Kant Healthcare Ltd. is inviting applications for the role of Officer – QA (QMS). If you are a qualified B.Pharm/M.Pharm graduate with 2–4 years of QA experience, this opportunity is your chance to contribute to a compliance-driven and growth-focused company.

Company Overview

S Kant Healthcare Ltd., established in 1932, is a trusted name in the pharmaceutical industry with decades of experience in manufacturing and delivering quality healthcare solutions. The company has a strong reputation for its commitment to Good Manufacturing Practices (GMP), innovation, and regulatory compliance. Over the years, S Kant Healthcare has consistently expanded its operations, catering to both domestic and global markets. Being a part of S Kant means contributing to a legacy of excellence in healthcare.

Job Role & Responsibilities

As an Officer – QA (QMS), you will be responsible for ensuring compliance across Quality Management Systems (QMS), with a focus on the following areas:

• Handling Annual Product Quality Reviews (APQR) to evaluate product performance and compliance.
• Managing Change Control processes to ensure proper documentation and approvals.
• Investigating and documenting Deviations in line with regulatory requirements.
• Coordinating with cross-functional teams to ensure quality standards are maintained.
• Supporting preparation for internal and external audits.
• Ensuring strict adherence to GMP, GLP, and company SOPs.

Eligibility / Qualifications

• Education: B.Pharm / M.Pharm.
• Experience: 2–4 years in QA (QMS).
• Skills Required:
  • Strong understanding of QMS processes (APQR, Change Control, Deviation management).
  • Knowledge of regulatory guidelines (USFDA, EU GMP, WHO).
  • Excellent documentation and compliance management skills.

Relevant Courses Include: B.Pharm, M.Pharm (Pharmaceutics, Quality Assurance, Pharmaceutical Technology).

Location & Salary

• Work Location: S Kant Healthcare Ltd. (Details provided by company).
• Salary: Competitive and as per industry standards.

Application Process

Interested and eligible candidates are encouraged to share their resumes directly with the HR team.

Email for Applications: hr@skant.com
Website: www.sk1932.com

Apply today to secure your chance to join S Kant Healthcare’s QA team and grow your career in pharmaceutical quality assurance!

FAQs

1. What is the eligibility for QA Officer roles at S Kant Healthcare?
B.Pharm/M.Pharm graduates with 2–4 years of QA (QMS) experience.

2. What QMS sections are included in this role?
APQR, Change Control, and Deviation management.

3. Can freshers apply for this role?
No, candidates must have at least 2 years of relevant QA experience.

4. What skills are essential?
Experience in QMS processes, knowledge of regulatory guidelines, and strong documentation practices.

5. How can I apply?
Send your updated resume to hr@skant.com.

6. Why join S Kant Healthcare?
S Kant offers a stable career with global exposure, a compliance-driven culture, and growth opportunities in pharmaceutical quality assurance.

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