Job Industry: Mechanical or Industrial Engineering
Job Type:
Full time
WorkPlace Type:
remote
Location: Abiquiu, New Mexico, United States
Job Description:
A well-known pharmaceutical firm situated at Islamabad, requires the services of skilled, competent and self-motivated individuals in the following capacities:
Ø Quality Control Analyst---02 Positions (Male/Female both are encouraged to apply)
Ø Location
Islamabad
a. Qualification:
B.Sc. /M.Sc. Chemistry/Pharm D
b. Experience:
2-3 years Proven experience in pharmaceutical manufacturing industry.
c. Skills Required:
Sampling and testing of raw materials, intermediates and finished products using current pharmacopoeias, any associated ‘wet’ chemistry and instrumental techniques (HPLC, IR, UV), as appropriate.
Preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports.
Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
Stability testing of products for new formulations and ongoing stability trials, using physical (pH,viscosity) and instrumental (HPLC, UV) techniques, as appropriate.
Writing analytical specifications using current pharmacopoeias and reviewing existing analyticalspecifications.
Writing/reviewing Standard Operating Procedures (SOPs).
Calibrating analytical equipment, as and when required.
Supporting all QC activities.
Ensuring that procedures are carried out carefully and accurately to eliminate errors.
Ensuring good relations and communications with all members of the team and responding politely andin a timely fashion to internal and external customers.
Working with all members of staff to maintain and develop the positive progressive culture within TheSpecials Laboratory.
Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
Observing and complying with company Health and Safety Policies.
Observing and complying with company Standard Operating Procedures (SOPs).
Undertaking any other duties, either for this department or any other department within the business, which may be requested by the Line Manager, for which training and/or an explanation has been provided and understood.
d. Handling & knowledge of:
1. HPLC, FT-IR,UV-Spectrophotometer, LPC, Polarimeter, Moisture analyzer.
2. Samples Testing & Analysis
3. Documentation Analytical Procedure
4. Testing of In-process control, finish goods & related documents.
5. Record maintenance of equipment & log book
6. Preperation of various QC reports.
7. Knowledge of method validation analysis and technical reports.
8. Commited towards job and long stay.