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Vacancies At Sanofi Pharmaceuticals - Quality Control And Production Positions  - vacanciesblog 2024
QA Qualification & Calibration Officer At Sanofi

Vacancies At Sanofi Pharmaceuticals – Quality Control And Production Positions 

Vacancies At Sanofi Pharmaceuticals –

Quality Control And Production Positions

1-Quality Control Analyst At Sanofi

Job Purpose:

The main purpose of this job is to perform routine and stability chemical analysis for products on daily basis according to the approved method of analysis.

Responsibilities and Tasks:

1- Performs all necessary testing procedure, issues Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.

2- Review all Obtained results for semi-finished products against the Out of trend limits and all the stability Results against the BIOST@T and ensure that all results are within the normal trends

3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Chemical lab head and the Q.C manager.

4- Sampling of semi-finished products, and ensures that sampling are conducting in full compliance with GLP and according to the instructions as per the SOP.

5- Perform Stability testing & assigned validation analysis tasks

6- Perform Printed packaging testing.

7- Fulfill other task(s) as assigned

8- HSE & Energy Contribution:

Ensures HSE approval on any SOP that requires certain HSE precautions. Ensures HSE approval on any change. Follow the laboratory safety procedures Commitment to the appropriate PPE use. Follow the approved HSE policy and requirements. Following the statutory legislation concerning Health, Safety and environmental law. Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system. Implement good calibration program for all instruments.

Supplementary Tasks:

● Utilizes, calibrates, maintains the QC equipment in the Chemical Lab according to the local SOP.

● Prepares relevant SOPs and follows up the update according to requirements.

● Performs other related duties as assigned.

● Makes sure that all activities carried on are complying with safety measurements.

● Updates methods of analysis.

● Respect of Company’s Values, Code of Ethics and Social Charter.

● Responsible for applying the HSE related requirements for the company in all working procedures

● Respect Personal Data Protection Charter.

Administration tasks in case of absence of the senior Administration Officer:

Receiving of Materials receipt records delivered from the warehouse for all batches of Raw, Aux, Primary packaging, & Printed packaging, , and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Receiving of Analysis Demands delivered from the production areas for all manufactured batches of semi-finished products, and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Checking of the Received printed packaging materials under the supervision of the Material and packaging material section head.
Responsible of preparation and adequate arrangement of all Q.C filling system and ensure correct and easy retrieval of any requested record and / or document.
Machines or Equipment Used:

All analytical instruments as per relevant analysis.

Job Holder Entry Requirements:

– Education: Bachelor Degree in Pharmacy, or Science

– Related Experience: experience in related positions. Experience in multinational companies will be considered.

– Special Knowledge/Skills:

Good command of English Language
Good computer skills
Familiar with new instrumental analysis techniques

Apply From Here


2-Sterile Production Pharmacist Professional (Project Based) At Sanofi

JOB PURPOSE:

Lead the Sterile production team in all the processes & operations with ensuring compliance with Sanofi quality standards & GMP and fulfilling the production plan.

On Project Basis (ends 30 Dec 2022)

KEY RESPONSIBILITIES AND DUTIES:

Participate in the GAP analysis of EU GMP Annex 1 Take the lead in implementation of the action plan resulting from the GAP analysis of EU GMP Annex 1 in the sterile production section Supervising Operators during the production process Assuring the process flow according to cGMP rules. Updating / Creating SOPs. Training New Operators on different Operations. Collection and Review of the Batch manufacturing records. Reporting any problems in utilities /machines during the production process Ensure that SANOFI products are complying to the quality measures and standards Follow up the area performance and put action plans for its improvement Respect of companies values, code of ethics and Social charter.

HSE & Energy Role:

Applying the machine safety checklist on regular basis. Ergonomics training on regular basis. Commitment to the appropriate PPE use Ensures that risk assessment to any new transferred product and new machine is adequately covered. Continuous monitoring to the first aid boxes Executing waste management measures for optimum utilization of resources. Follow the approved HSE policy and requirements. Follow all the statutory legalization concerning Health, Safety and environmental law.

HSE Responsibilities in case joining HSE Excellence team:

Facilitate and guide the employees to implement the HSE&En. Policies. Implement all applicable standards and guides of Sanofi-Aventis in his/her area. Ensure from complying with all legal and Sanofi-Aventis requirements. Lead his/her team to implement the HSE & EnMS PASS. Train his/her team on HSE & EnMS procedures, SOP’s and MSDS. Report any accidents/incidents in his/her area to the HSE department. Lead his/her team for investigate accidents/incidents to define the root cause. Support the area manager for takes the corrective and preventive actions to eliminate reoccurrence of any Environmental or Energy nonconformance. Support the area manager for takes the corrective and preventive actions to eliminate reoccurrence of any accident/incident. Sharing for HSE / EnMS inspection program, take the corrective actions for any violations in his/her area. Lead the team of his/her area for doing full risk assessment and Environmental aspects studies. Define and control the required PPE’s for his/her area. Define the list of CMR and it’s operational control for Quality labs and production areas. Control the first aid kits in his/her area. Leading his/her team for control the significant hazards /aspects and Energy use.

Others:

Perform other duties as assigned.
Respect of company’s values, code of ethics and social charter.
Respect of personal data protection charter.
Responsible for applying the HSE related requirements for the company in all related working procedures.
Education:

Bachelor Degree in Pharmacy
Related Experience:

6 months – 2 years of experience in Pharmaceutical Company
Special Knowledge/Skills:

Leadership skills.
Good communication and negotiation skills.
Problem solving skills.
Excellent Computer skills.
Excellent Command of English.
competencies:

Stretch to go beyond the level we have operated at up until now
Take actions instead of waiting to be told what to do
Act in the interest of our patients and customers
Put the interests of the organization ahead of my own or those of our team

Apply From Here


3-Senior Quality Control Analyst At Sanofi

job description

1- Performs all necessary testing procedure, issues Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.

2- Review all Obtained results for semi-finished products against the Out of trend limits and all the stability Results against the BIOST@T and ensure that all results are within the normal trends

3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Chemical lab head and the Q.C manager.

4- Sampling of semi-finished products, and ensures that sampling are conducting in full compliance with GLP and according to the instructions as per the SOP.

5- Perform Stability testing & assigned validation analysis tasks

6- Perform Printed packaging testing.

7- Fulfill other task(s) as assigned

8- HSE & Energy Contribution:

Ensures HSE approval on any SOP that requires certain HSE precautions. Ensures HSE approval on any change. Follow the laboratory safety procedures Commitment to the appropriate PPE use. Follow the approved HSE policy and requirements. Following the statutory legislation concerning Health, Safety and environmental law. Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system. Implement good calibration program for all instruments.

Supplementary Tasks:

● Utilizes, calibrates, maintains the QC equipment in the Chemical Lab according to the local SOP.

● Prepares relevant SOPs and follows up the update according to requirements.

● Performs other related duties as assigned.

● Makes sure that all activities carried on are complying with safety measurements.

● Updates methods of analysis.

● Respect of Company’s Values, Code of Ethics and Social Charter.

● Responsible for applying the HSE related requirements for the company in all working procedures

● Respect Personal Data Protection Charter.

Administration tasks in case of absence of the senior Administration Officer:

Receiving of Materials receipt records delivered from the warehouse for all batches of Raw, Aux, Primary packaging, & Printed packaging, , and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Receiving of Analysis Demands delivered from the production areas for all manufactured batches of semi-finished products, and recording them in Q.C samples receipt record, and delivers them to Q.C samplers to start sampling and analysis processes
Checking of the Received printed packaging materials under the supervision of the Material and packaging material section head.
Responsible of preparation and adequate arrangement of all Q.C filling system and ensure correct and easy retrieval of any requested record and / or document.
Requirements:

Education: Bachelor Degree in Pharmacy, or Science

Related Experience: 5- 7 years experience in related positions, preferably in multinational company.

Special Knowledge/Skills:

command of English Language
Good computer skills

Apply From Here

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