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Hiring: Laurus Labs (API Production, QC & Synthesis R&D)


Hiring: Laurus Labs (API Production, QC & Synthesis R&D)

For pharmaceutical professionals seeking direct email application opportunities, Laurus Labs Limited—a leading research-driven pharmaceutical and API manufacturing company—is accepting direct resume submissions for key operational and R&D roles at its Visakhapatnam and Hyderabad facilities.

Here is a structured overview of this direct pharmaceutical opening for your blog:

📌 Role & Location Overview

  • Company: Laurus Labs Limited
  • Plant & R&D Locations: Visakhapatnam (Vizag) & Hyderabad, Andhra Pradesh / Telangana
  • Departments: API Production, Quality Control (QC), and Synthesis R&D / Process Chemistry
  • Positions: Chemist / Executive / Senior Scientist
  • Experience Required: 1 to 7 Years
  • Application Mode: Direct Email CV Submission

🎯 Active Vacancies & Requirements

1. API Production & Manufacturing Operations

  • Qualifications: B.Sc / M.Sc (Chemistry) / Diploma in Chemical Engineering
  • Experience Required: 1 to 5 Years
  • Core Skills: Operating reactors (SSR/GLR), centrifuges, dryers (FBD/RCVD), and micronizers in API plants. Ensuring cGMP compliance, safety protocol implementation, and maintaining Batch Production Records (BPR).

2. Quality Control (QC) – API & Intermediates

  • Qualifications: M.Sc (Analytical / Organic Chemistry) / B.Pharm
  • Experience Required: 2 to 6 Years
  • Core Skills: Method execution and routine testing of raw materials, in-process, and finished active pharmaceutical ingredients. Hands-on expertise with HPLC, GC, LC-MS, wet chemical analysis, and lab data integrity tools.

3. Synthesis R&D / Process Development

  • Qualifications: M.Sc (Organic Chemistry) / Ph.D.
  • Experience Required: 2 to 7 Years
  • Core Skills: Route scouting, process optimization, scale-up of novel intermediate synthesis, handling hazardous reagents safely, and technical transfer to manufacturing units.

📋 Resume Submission Guidelines

When submitting your application via email, ensure your CV includes:

  • Specific scale of operation or chemistry expertise (e.g., API scale-up, specific analytical software used).
  • Clear employment history detailing major regulatory plant exposure.
  • Current CTC, expected salary, current residence, and official notice period.

📬 How to Apply (Direct Email Application)

Eligible candidates can send their updated resume directly to the Laurus Labs HR talent team:

📧 Email CV to: talents@lauruslabs.com (Subject Line Format: "Application for [Department] - [Position Title] - [Years of Experience]")

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Hiring: Cadila Pharmaceuticals (QA Validation, Analytical R&D & Regulatory Affairs)


Hiring: Cadila Pharmaceuticals (QA Validation, Analytical R&D & Regulatory Affairs)

For pharmaceutical professionals and researchers looking for non-walk-in, direct email applications, Cadila Pharmaceuticals Limited—one of India's premier healthcare and API/formulation companies—is accepting direct resume submissions for multiple specialized technical openings.

Below is a structured overview of these direct positions for your blog:

📌 Role & Location Overview

  • Company: Cadila Pharmaceuticals Limited
  • Locations: Dholka (Ahmedabad) & Bhat (Gandhinagar), Gujarat
  • Departments: Quality Assurance (Validation), Analytical R&D (API), and Regulatory Affairs (RA)
  • Experience Required: 2 to 9 Years
  • Application Mode: Direct Email CV Submission

🎯 Technical Positions & Requirements

1. QA Executive – Process & Equipment Validation

  • Location: Dholka Plant, Ahmedabad
  • Qualifications: B.Pharm / M.Pharm / M.Sc
  • Experience Required: 3 to 7 Years
  • Core Responsibilities: Preparing and executing Process Validation, Cleaning Validation, and Equipment Qualification protocols for oral solid dosage (OSD) and injectable lines.

2. Research Scientist – Analytical R&D (API)

  • Location: R&D Center, Bhat, Gandhinagar
  • Qualifications: M.Sc (Analytical / Organic Chemistry) / M.Pharm
  • Experience Required: 4 to 9 Years
  • Core Responsibilities: Method development and validation for active pharmaceutical ingredients (APIs) using HPLC, GC-MS, LC-MS, and handling structure elucidation.

3. Officer / Executive – Regulatory Affairs (DRA)

  • Location: Corporate Campus, Bhat
  • Qualifications: B.Pharm / M.Pharm
  • Experience Required: 2 to 5 Years
  • Core Responsibilities: Dossier preparation (eCTD format), filing regulatory submissions for semi-regulated and regulated markets, and managing query responses.

📋 Resume Submission Guidelines

When submitting your application via email, ensure your CV includes:

  • Explicit details of regulatory guidelines handled (e.g., USFDA, EU-GMP, WHO).
  • Current company details, designations held, and notice period.
  • Updated contact details and key technical tools/instruments used.

📬 How to Apply (Direct Email Application)

Eligible candidates can email their updated CV directly to the Cadila HR talent acquisition team:

📧 Email CV to: talent.acquisition@cadilapharma.co.in (Subject Line Format: "Application for [Position Title] - [Department] - [Years of Experience]")

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Walk-in For Production,QA,QC,R&D, Purchase And ADL Departments At SIMPEX PHARMA

WALK-IN INTERVIEW

Production, QA, QC, R&D, Purchase & ADL

Simpex Pharma Pvt. Ltd. is a leading, international pharmaceutical company, producing a wide range of medicines, backed by constant research & innovation, which are trusted by health care professionals & patients across the globe.

Simpex Pharma is having following Regulatory Affairs approvals such as:

USFDA Certification

• Ukraine GMP

• Ethiopia GMP

DIGEMID Certification

• Philippines GMP

• Ivory Coast GMP

Yemen GMP

• Russia MОН

• WHO GMP

Documents Required: Please carry your Legible Documents Like Updated CV, Passport Size Photo, Copies of Education Documents, Aadhar & PAN, Latest CTC Documents, 3 Months Payslips, 3 Month bank Statement

Haridwar (Hotel Hyphen)

Job Location: Kotdwar

Date: 20th October 2024 (Sunday) Time- 10:00 Hrs To 16:00 Hrs

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Hiring For Research And Development Department At Sun Pharma

The R&D (Research and Development) department in the pharmaceutical industry plays a critical role in discovering, developing, and bringing new drugs and treatments to market. This department is responsible for:

1. Drug Discovery: 
   - Identifying new molecules or compounds with therapeutic potential. 
   - Screening for biological activity that can treat specific diseases.
   - Understanding disease mechanisms and target identification.

2. Preclinical Research:
   - Conducting laboratory and animal studies to evaluate the safety, efficacy, and pharmacological profile of the candidate drug.
   - Studying the drug’s pharmacokinetics (how the body absorbs, distributes, metabolizes, and excretes the drug) and pharmacodynamics (the drug’s effects on the body).

3. Clinical Trials:
   - Managing and conducting clinical trials across different phases (Phase I, II, III, and IV) to evaluate safety, dosage, side effects, and efficacy in humans.
   - Ensuring regulatory compliance during the trials.

4. Regulatory Affairs:
   - Preparing and submitting data to regulatory authorities (e.g., FDA, EMA) to get approval for clinical trials and marketing of the drug.
   - Interfacing with regulatory bodies to ensure the drug meets all legal and safety standards.

5. Process Development:
   - Developing scalable and efficient manufacturing processes for the drug.
   - Optimizing the production to ensure consistent quality and safety.

6. Innovation and Technology:
   - Utilizing cutting-edge technologies such as artificial intelligence (AI), machine learning, and biotechnology to enhance drug discovery and development.
   - Investing in personalized medicine, gene therapy, or biologics for more targeted therapies.

7. Post-Marketing Surveillance:
   - Monitoring the drug’s performance in the market (Phase IV studies) to identify any long-term effects or rare side effects that weren’t detected during earlier trials.

8. Collaborations:
   - Partnering with academic institutions, biotech companies, and other pharmaceutical firms to share resources and knowledge, accelerating innovation.

The R&D process is complex, expensive, and time-consuming but essential for advancing medical treatments and addressing unmet medical needs.

We are hiring Apply now

Funtion: R&D Formulation Development- Orals
Job Location: Baroda
Grade: Executive/ Sr Executive
Qualification & Experience: M.Pharm having 3 - 6 yrs in R&D Formulation 
Development - Orals

Send your resume to:
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Tagoor Laboratories Pvt Ltd Walk in interview for Fresher's and Experience for R&D and AR&D department

Tagoor Laboratories Pvt Ltd Walk in interview for Fresher's and Experience for R&D and AR&D department on 09-10-2024 (Wednesday)

Walk in interview for Fresher's and Experience Candidates

WALK IN INTERVIEWS FOR - R&D & AR&D (SYNTHESIS)

Department: R&D and AR&D

Experience: 0 to 8 years

Qualification for Fresher's MSC, B.Sc-Organic/ Chemistry/ Analytical

Qualification for Experience Any PG/ Any Degree

Experience: 0 to 8 Years

No. Of Positions: 25

Work location: Jeedimetla

Date: 09-10-2024 (Wednesday)

Venue: Plot No: 121,122 & 130,131, Phase-I, SVCIE IDA Jeedimetla, Quthbullapur (M), Medchal - Malkajgiri (D), Hyderabad- 500055

Please carry your documents:

All Educational Certificates

Last 3 Months Payslips

Last 3 Months bank statement

Recent increment Letter

Aadhar Card

Pan Card

EPF Service Copy

Interested candidates can share their CV on career@tagoor.com, Contact: 9100990040
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Opening For Research And Development And Packing Department At Sun Pharma

R&D Packaging Development -

Non Orals

Job Location: Baroda

Grade: Manager

Job Description:

1. Characterization of RLD Pack samples for injectable, ophthalmic and inhalation products.

2. Finalization of pack configuration for exhibit batches of new generic products/ NDA products as per requirement.

3. Identification of new packaging materials and new vendor development for packaging materials.

4. Mold development for primary & secondary packaging materials and its validation.

5. Support to regulatory team for ANDA's / NDA's filling for regulated market & support for query response.

6. Coordination with NPI and planning team for launch of ANDA's / NDA's

Please share your resume at: Rosemary.varghese@sunpharma.com
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Walk-in interview For R&D And AR&D Departments At Tagoor Laboratories Pvt Ltd

Tagoor Laboratories Pvt Ltd

WALK IN INTERVIEWS FOR - R&D & AR&D (SYNTHESIS)

Qualification for Fresher's MSC, BSC-Organic/Chemistry/Analytical

Qualification for Experience Any PG/Any Degree

Experience 0 to 8 Years

No. Of Positions 25

Please carry your documents:
All Educational Certificates
Last 3 Months Payslips
Last 3 Months bank statement
Recent increment Letter
Aadhar Card
Pan Car
EPF Service Copy

View Job Details