π¬ Accuprec Research Labs β Pharma Jobs Ahmedabad 2026 π¬
π§ͺ QA, QC, R&D, Regulatory Affairs, Business Development | HPLC LCMS | 2β17 Years
π Explore top pharma jobs at Accuprec Research Labs with roles in QA, QC, R&D, and regulatory affairs. Apply now for rewarding pharmaceutical careers in India.
π’ About the Company
π Accuprec Research Labs Pvt. Ltd. is a fast-growing pharmaceutical research organization known for its expertise in analytical testing, regulatory compliance, and contract research services.
π The company operates with global standards, adhering to ICH, USFDA, EMA, and other regulatory bodies.
π¬ With a strong focus on innovation, quality, and scientific excellence, Accuprec offers a dynamic environment for professionals seeking long-term growth in pharmaceutical careers in India.
πΌ Job Details
- π’ Company Name: Accuprec Research Labs Pvt. Ltd.
- β³ Experience: 2β17 Years (varies by role)
- π Qualification: M.Sc, M.Pharm, BBA, MBA, B.E, B.Tech, M.Tech, Ph.D, MLT, DMLT
- π Location: Ahmedabad, Gujarat, India
- π Work Type: On-site
π Job Description
π’ Accuprec is hiring across multiple departments including Analytical Development (AD), Quality Control (QC), Regulatory Affairs, Business Development, and Project Management.
π― These pharma jobs are ideal for candidates with strong technical expertise and industry experience.
π§ͺ Research Associate / Sr. Research Associate β HPLC (AD Department)
- π Department: Analytical Development
- π¬ Role: Method Development & Validation
- β³ Experience: 3β7 Years
- π Qualification: M.Sc / M.Pharm
π Business Development Executive
- π Department: Business Development
- π Role: Sales, Lead Generation & Strategy
- β³ Experience: 3β8 Years
- π Qualification: BBA / MBA (Marketing)
𧬠Sr. Research Associate β LCMS
- π Department: AD & QC
- βοΈ Role: Nitrosamine Analysis & LC-MS/MS
- β³ Experience: 4β6 Years
- π Qualification: M.Sc / M.Pharm (Analytical Chemistry)
π§ Manager β Mechanical Engineering
- π Department: Mechanical
- π Role: Engineering Design & Project Leadership
- β³ Experience: 10β17 Years
- π Qualification: B.E / B.Tech / M.Tech / Ph.D
π Research Associate β Pharmacology & Toxicology
- π Department: Pathology
- π¬ Role: Preclinical & Clinical Research Support
- β³ Experience: 2β4 Years
- π Qualification: MLT / DMLT
π Executive / Sr. Executive β Project Management
- π Department: Project Management
- π Role: Project Coordination & Client Communication
- β³ Experience: 5β8 Years
- π Qualification: M.Sc / M.Pharm
π Regulatory Affairs Specialist (New Venture)
- π Department: Regulatory Affairs
- π Role: CTD/eCTD Dossier Preparation
- β³ Experience: 3β5 Years
- π Qualification: M.Pharm (Regulatory Affairs)
β Regulatory Query Response Officer / Executive
- π Department: Regulatory Affairs
- π Role: Query Handling & Compliance
- β³ Experience: 3β5 Years
- π Qualification: M.Pharm
π¬ Study Director β Analytical Development
- π Department: Analytical Development
- π§ͺ Role: Validation, E&L, Bioanalytical Studies
- β³ Experience: 4β6 Years
- π Qualification: M.Pharm / M.Sc
π§ Skills/Qualifications
- π§ͺ Strong knowledge of HPLC, LC-MS/MS, UV, IC, Dissolution
- π Expertise in analytical method validation (ICH guidelines)
- π Experience in regulatory submissions (CTD/eCTD)
- π Understanding of USFDA, EMA, ICH, CDSCO norms
- π Project management and cross-functional coordination
- π€ Business development and client handling skills
- π Excellent communication and documentation abilities
- β οΈ Knowledge of nitrosamine impurity assessment
π οΈ Key Responsibilities
- π¬ Develop and validate analytical methods
- π§ͺ Perform forced degradation studies
- π Manage regulatory documentation and submissions
- β οΈ Conduct nitrosamine risk assessments
- π€ Coordinate cross-functional project activities
- π Handle client communication and reporting
- 𧬠Execute bioanalytical and pharmacokinetic studies
- β Ensure compliance with global guidelines
π Benefits/Perks
- π Professional growth opportunities
- π€ Collaborative work environment
- π° Competitive compensation
- π Exposure to global regulatory standards
- π Learning and development programs
- π Stable pharmaceutical career path
π© How to Apply
π§ Interested candidates can apply by sending their updated resume to: [email protected]
π For queries, contact: +91 9512660923
π Why You Should Join
π Accuprec Research Labs offers a strong platform for career advancement in pharma jobs, QA jobs, QC jobs, and regulatory roles.
π Employees benefit from a culture of innovation, compliance-driven operations, and continuous learning.
π¬ With exposure to global standards and cutting-edge research, professionals can build a stable and rewarding career.
β FAQs
1. What is the eligibility for Accuprec pharma jobs?
A: Candidates must have relevant degrees like M.Sc, M.Pharm, MBA, or engineering qualifications with required experience.
2. How can I apply for these roles?
A: You can apply by emailing your resume to [email protected] or contacting the provided numbers.
3. Are walk-in interviews available?
A: No walk-in interview details are mentioned. Applications are accepted via email.
4. What career growth opportunities are offered?
A: Accuprec provides learning programs, global exposure, and long-term career development in pharmaceutical domains.
Apply now and accelerate your career in the pharmaceutical industry!
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