Vacancies At BioGeneric Pharma

BioGeneric Pharma S.A.E: a leading factory in biotechnology in the Middle East, is seeking to hire “Stability Supervisor” with the following requirements:

JOB SUMMARY

Follows up, coordinates and performs lab analytical procedures for IPC samples and drug products, following BGP procedures, GMP and GLP guidelines

Responsibilities:

·        Issue raw materials lab SOPs/procedures for test activities & lab instruments use and maintenance.

·        Follow up and write SOPs for stability according to company procedures and cGMP requirements.

·        Follow up and carry out laboratory duties and analytical procedures according to issued SOPs and cGMP requirements.

·        Operation, maintenance, and cleaning of stability chambers.

·        Follow up on Qualification, Calibration & Maintenance of stability chambers.

·        Follow up stability studies according to stability study plans

·        Manages, handles and analyzes stability samples.

·        Create stability study protocols.

·        Create stability study reports.

·        Ensure documenting all activities according to cGMP.

·        Document and communicate any incidents or deviations, according to relevant SOPs & forms.

·        Other relevant duties may be performed.

Experience:

·     Minimum 4 years’ experience (pharmaceutical, cosmetics, or biopharmaceutical company).

Education: Bachelor’s degree in pharmacy, science (chemistry; major or minor), or relevant degree

Skills and Knowledge

§ Strong leadership and management skills

§ Excellent communication and interpersonal skills

§ Strong analytical and problem-solving skills

Interested and qualified candidates are encouraged to send their updated CVs to: hr@bioGenericpharma.com

Quoting the job title “Stability Supervisor” in the subject field.

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BioGeneric Pharma S.A.E: a leading factory in biotechnology in the Middle East, is seeking to hire “Raw / Packaging materials Supervisor” with the following requirements:

JOB SUMMARY

Follows up, coordinates and performs lab analytical procedures for IPC samples and drug products, following BGP procedures, GMP and GLP guidelines

Responsibilities:

·        Issue raw materials lab SOPs/procedures for test activities & lab instruments use and maintenance.

·        Analyze raw, packaging materials and waters samples.

·        Follow up & train RM lab technicians and analysts on different analytical methods & documentation system inside raw/packaging materials lab.

·        Receive and review receival of raw/ packaging materials samples according to relevant standard operation procedures.

·        Perform and review various testing procedures / SOPs related to RM lab.

·        Support lab analysts & technicians via technical problems solving.

·        Participate & follow up various safety instructions and maintain a safe work area.

·        Manage incoming samples (raw materials materials) to ensure testing on time.

·        Review the preparation of all required reagents, volumetric solutions, indicators & other solutions required for analysis.

·        Review the validity of prepared solutions/standards before use.

·        Initiate & follow up purchase requests related to RM lab.

·        Apply lab procedures related to expired, deteriorated, spoiled, or consumed chemicals.

·        Assist lab supervisor in laboratory investigation in case of out of specifications or out of trend.

·        Participating in validation, verification and qualification programs related to QC-CPRMTL raw materials lab.

·        Review the validity of any analytical instrument before use.

·        Review & follow up the storage system of all chemicals, prepared reagents and reference standards.

·        Follow up cleanliness of equipment and working area.

·        Perform & review verification or calibration of instruments/ equipment according to the approved procedures and schedule.

·        Issue & Update SOP & related forms/attachments for test activities & lab instruments according to Up-to-date guidance.

·        Review recording in the relevant documents according to issued SOPs/procedures & related lab documents.

·        Review results report & certificate of analysis.

·        Perform trend analysis & related documentation

·        Other relevant duties may be performed.

Experience:

·     2 – 4 years experience (pharmaceutical, cosmetics, or biopharmaceutical company).

Education: Bachelor’s degree of bachelor degree of pharmacy, science (chemistry; major or minor), or relevant degree

§ Skills and Knowledge

§ Strong leadership and management skills

Interested and qualified candidates are encouraged to send their updated CVs to: hr@bioGenericpharma.com

Quoting the job title “Raw/Packaging materials Supervisor” in the subject field.