Sami Group is in Pharma, Life Sciences & Health care domain around 27 years. We have 100+ Patents, numerous trademarked ingredients, Offices in 9 countries, 5 manufacturing units in India, 1 manufacturing unit in USA, 5 R&D labs, nearly 40,000 acres of cultivation through contract farming and 1000+ employees. We are well known as Sami Labs in India and Sabinsa across the world. For more details, you can refer to
The websites of our other group companies are: , , ,

Sr. Manufacturing Manager / Manufacturing Manager
    Experience: About 10 years in a dosage manufacturing facility at a supervisory level.
    Desired Qualification: Ph.D in Chemistry, Pharmaceutical or Chemical Technology
    Dosage forms handled: Solid, Semisolid & Liquid formulations.

    Desired Profile:

    1. Should be well versed with various processes & equipments involved in manufacturing of different pharmaceutical dosage forms.

    2. Competent in all unit operations associated with different oral & cosmetic formulations including stability studies.

    3. Experience in scale-up & technology transfer of finished dosage forms.

    4. Knowledge of GMP & Regulatory requirements.

    5. Sound communication, presentation & coordination skills at all levels & across functions.

    6. Knowledge of Risk management and avoidance of wastages in formulations

    7. Experience in Time Management and Adhering to the production planning and schedules.

    8. Preparation and maintenance of production documents and adequate computer knowledge.
    QC Manager / Senior QC Manager
        The candidate should be a Ph.D having minimum 10 Years of experience in the Quality Control or in an analytical R&D facility of a reputed organisation.
        Should have good knowledge and hands on experience in handling various analytical instruments like HPLC, GC, UV spectrophotometer, IR, viscometer and other basic analytical instruments along with their calibration and .
        Should have exposure towards analysing various types of formulations and dosage forms like tablets, capsules, creams, Lotions and other similar formulations including their stability testing.
        Should have worked in a GLP certified facility with a knowledge of setting up a lab or making improvements in the existing infrastructure. This would be an added advantage.
        Candidate should have an ability to manage analytical tasks related to natural products using various chromatographic methods including preparative methods.
        Should have knowledge in documentation of the analytical records, Certificate of analysis, analytical methodologies and other related requirements of the department.
        Exposure towards customer and regulatory Audits/ requirements would be an added advantage.
        The Applicant should have excellent communication and presentation skills.
        Recruiter Name:Snehal

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