ADL Manager (Ahmedabad)

ADL Manager (Ahmedabad)

19 Oct
|
Sushen Medicamentos
|
Ahmedabad

19 Oct

Sushen Medicamentos

Ahmedabad

Company Description Sushen Medicamentos Pvt. Ltd. is an EU-GMP certified partner for global pharmaceutical companies, providing end-to-end product management and formulation development services. The company specializes in pharmaceutical plant design, implementation, equipment procurement and qualification, and engineering services in line with international regulatory requirements such as WHO-GMP, USFDA, and EU GMP norms.

Sushen offers comprehensive support, including documentation systems, cGMP compliance, product registration, and commercial batch trials. It also provides formulation and development services for oral solid dosage forms, stability and dissolution studies, and BA/BE study organization. With a WHO-GMP certified, DSIR-approved, state-of-the-art laboratory and a team of experienced engineers and pharmacists, Sushen has successfully executed over 40 projects across the US, Europe, CIS, Middle East, Latin America, Africa, South East Asia, and India.

Role Description The ADL Manager is a full time, on-site role based in Ahmedabad, responsible for managing and overseeing Analytical Development Laboratory activities. This role includes planning, supervising, and reviewing analytical method development and validation for pharmaceutical products, ensuring adherence to regulatory and cGMP requirements. The ADL Manager will coordinate with formulation, production, and quality teams, monitor laboratory workflows, and ensure timely completion of projects and studies.

Responsibilities also include maintaining laboratory documentation,



supporting audits and inspections, implementing continuous improvement initiatives, and training and mentoring laboratory staff. The ADL Manager will collaborate with cross-functional teams to support tech transfer, stability studies, and product registration activities.

Qualifications

- Candidates should possess strong expertise in analytical method development, validation, and stability study management within pharmaceutical or CDMO environments.
- Candidates should possess skills in managing laboratory operations, including workflow planning, resource allocation, and oversight of instrumentation and equipment maintenance.
- Candidates should possess knowledge of cGMP, regulatory guidelines (e.g., WHO-GMP, USFDA, EU-GMP), and documentation practices for audits, product registration, and quality systems.
- Candidates should possess abilities in cross-functional collaboration, team leadership, staff training, and performance monitoring in a laboratory setting.
- Candidates should possess strong analytical thinking, problem-solving skills, attention to detail, and proficiency with relevant analytical tools and software.
- Master’s or Bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline is preferred; prior experience in analytical development or quality control in the pharmaceutical industry is highly beneficial.
- Ability to work on-site in Ahmedabad, adapt to dynamic project needs, and communicate effectively in written and spoken English.

📌 ADL Manager (Ahmedabad)
🏢 Sushen Medicamentos
📍 Ahmedabad

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