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  • Posted: Jun 4, 2020
    Deadline: Jun 10, 2020
  • We are widely valued for providing our clients with ISO Consultancy Services. Rendered by diligent professionals, these offered services are appreciated for their time-execution, reliability and authenticity. During the dealings, we assure that all the rules and regulations are followed as per the International norms.
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    Job Description

    • Investigated causes of failures and developed new procedures for problem-solving to produce a high-quality product and maximize output.
    • Worked independently performing troubleshooting, staff mentoring, and object-oriented research and analysis.
    • Maintained validation summaries and standard operation procedures to ensure compliance with cGMPs.
    • Performed routine duties on bulk & in-process personal care samples and finished goods.
    • Major contributor to the efficient transfer and release of products from compounding to production.
    • Participated in cross-training in the Raw Materials and HPLC departments.
    • Successfully introduced a new and more effective finish goods batch coding/tracking system.
    • Conducted investigations on questionable/problematic batches and documented findings.
    • Wrote and help implement SOP and methods in Quality Control department
    • Used detailed manufacturing instructions and SOPs to complete assigned production activities according to quality standards
    • Documented and maintained records and notebooks in a neat, thorough, and accurate manner
    • Operated laboratory equipment safely, as trained and directed others in accordance to established procedures

    Your Profile

    • Revised and updated SOPs as needed
    • Minimum of 5 years’ work experience
    • Bachelor's Degree in Chemistry or related field
    • Experienced in cGMP manufacturing
    • Maintaining good housekeeping
    • Excellent written and oral communication skills
    • Communicate effectively and ability to function well in a team environment
    • Ability to communicate in a proactive and solution-focused manner, including keeping direct supervisor aware of potential issues
    • Flexibility of working hours based on business needs, may include some nights and occasional weekends
    • Ability to work independently and manage one’s time
    • Ability to effectively organize, multitask, and work in a fast-paced, deadline-driven work environment
    • Detail-oriented with the ability to troubleshoot and resolve problems
    • Good computer knowledge, including Microsoft Word, Excel and PowerPoint
    • Experienced using analytical HPLC/UPLC, prep HPLC system, lyophilizers, balances, solid as well as liquid phase reactors, HF cleavage equipment, diafiltration systems, water purification systems, oven, washing systems and other equipment used in manufacturing
    • Experienced in working in a cleanroom environment (ISO 7 & ISO 8 classified rooms)
    • Capable of qualifying equipment and performing routine maintenance on equipment

    Method of Application

    Interested and qualified candidates should send their CV to: using the "Job Title" as the subject of the email.

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