Adaptis Life Sciences Hiring Regulatory, PV & BD

Adaptis Life Sciences Regulatory, PV & BD Openings – Hyderabad

M.Pharm/M.Sc/B.Pharm/MBA openings in Regulatory Affairs, Pharmacovigilance & Business Development.

Adaptis Life Sciences is inviting qualified professionals to join its Regulatory Affairs, Pharmacovigilance, and Business Development teams. With opportunities across mid-level and entry positions, this hiring drive offers career growth for candidates with expertise in regulatory submissions, case processing, and digital marketing within the pharma domain.

Company Overview

Adaptis Life Sciences is a fast-emerging pharmaceutical service provider offering regulatory consulting, pharmacovigilance, and clinical support to global clients. With a strong focus on innovation, compliance, and operational excellence, Adaptis enables pharmaceutical and biotech companies to navigate complex international regulatory environments.

The company operates with a mission to simplify drug approval processes and ensure patient safety by delivering reliable and compliant solutions. Adaptis’ integrated service model combines Regulatory Affairs, Pharmacovigilance, and Business Development expertise — making it a trusted partner for pharmaceutical success.

Job Role & Responsibilities

Regulatory Affairs – Assistant Manager (ANDA/NDA & BLA Modules)

Experience: 4–9 years
Qualification: M.Pharm / M.Sc (Pharmaceutical Sciences, Regulatory Affairs, Chemistry)

Key Responsibilities:

• Compile and review regulatory submission documents for ANDA/NDA/BLA modules.
• Manage query responses from global health authorities (USFDA, EMA, MHRA, etc.).
• Coordinate with formulation, QA, and clinical teams for dossier preparation.
• Maintain regulatory tracking systems and document databases.
• Review labeling, CMC data, and variation filings.

Preferred Skills:

• Strong knowledge of CTD/eCTD submission formats.
• Hands-on experience in lifecycle management and post-approval changes.
• Ability to manage timelines and coordinate with multiple stakeholders.

Pharmacovigilance – Executive

Experience: 3–4 years
Qualification: M.Pharm / M.Sc (Pharmacology, Clinical Research, Life Sciences)

Key Responsibilities:

• Perform case intake, narrative writing, coding, and case processing using safety databases.
• Conduct medical review support and ensure compliance with safety reporting timelines.
• Identify and report adverse events following global PV regulations.
• Collaborate with QA and medical teams to ensure compliance with SOPs.

Preferred Skills:

• Experience in global pharmacovigilance systems (e.g., Argus, ArisG, Safety Database).
• Strong understanding of ICH-GCP, MedDRA coding, and PSUR/DSUR documentation.
• Excellent written and analytical communication.

Business Development – Executive

Experience: 0–1 year (Freshers eligible)
Qualification: B.Pharm / MBA (Marketing / Pharmaceutical Management)

Key Responsibilities:

• Identify new business opportunities in pharmaceutical services.
• Support client communication, proposals, and lead generation.
• Assist marketing and digital campaigns for brand outreach.
• Collaborate with project management and regulatory teams for client coordination.

Preferred Skills:

• Excellent communication and presentation skills.
• Basic understanding of pharma business models.
• Knowledge of digital marketing tools preferred.

Eligibility / Qualifications

Required Education: M.Pharm, M.Sc, B.Pharm, MBA
Relevant Courses (comma-separated): M.Pharm Regulatory Affairs, M.Pharm Pharmaceutics, M.Sc Life Sciences, M.Sc Pharmacology, M.Sc Chemistry, B.Pharm, MBA Pharmaceutical Management, MBA Marketing, PG Diploma in Pharmacovigilance, PG Diploma in Regulatory Affairs

Experience: 0–9 years (role-dependent).
Freshers can apply for Business Development roles; Regulatory and PV positions require prior experience.

Location & Salary

Location: Hyderabad, Telangana
Salary: Competitive and based on qualification and experience.
Experienced professionals in Regulatory Affairs and PV can expect industry-standard packages with performance incentives.

Application Process

Interested candidates can send their updated resumes to:
info@adaptisls.com

Shortlisted applicants will be contacted for interviews. Ensure to mention the applied position (e.g., “Regulatory Affairs – Assistant Manager” or “Pharmacovigilance Executive”) in the subject line.

Key Highlights (Why Join Adaptis Life Sciences)

• Exposure to international regulatory submissions and PV case management.
• Opportunity to work on complex injectable and novel formulation projects.
• Fast-growing, innovation-driven environment with global client exposure.
• Career advancement opportunities in multidisciplinary pharma operations.
• Inclusive workplace encouraging professional skill development.

FAQs

Q: What are the qualifications required for Regulatory Affairs roles?
A: M.Pharm or M.Sc in Regulatory Affairs, Pharmaceutics, or Chemistry with 4–9 years of experience.

Q: Are freshers eligible for any roles?
A: Yes, freshers can apply for Business Development Executive positions.

Q: What is the work location?
A: Hyderabad, Telangana.

Q: How can I apply?
A: Send your CV to info@adaptisls.com with your role mentioned in the subject line.

Q: Is there an interview process?
A: Shortlisted candidates will be called for technical and HR interviews.

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Vertical Summary Table

+------------------------------+----------------------------------------------------------------+
| Company                      | Adaptis Life Sciences Pvt. Ltd.                                 |
+------------------------------+----------------------------------------------------------------+
| Vacancies                    | Regulatory Affairs (Asst. Manager), Pharmacovigilance (Executive),|
|                              | Business Development (Executive)                                |
+------------------------------+----------------------------------------------------------------+
| Required Education           | M.Pharm, M.Sc, B.Pharm, MBA                                     |
+------------------------------+----------------------------------------------------------------+
| Experience                   | 0–9 years (role-based)                                          |
+------------------------------+----------------------------------------------------------------+

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