PHARMACEUTICAL ASSOCIATES

PHARMACEUTICAL ASSOCIATES, a manufacturer of liquid pharmaceuticals, is accepting resumes at their Greenville, SC facility for these positions: VALIDATION TECHNICIAN To assist in validating manufacturing processes, documenting results, performing cleaning validations, and equipment qualifications. Position requires attention to detail and Chemistry or related sciences degree is preferred. Candidate must have technical writing ability. Previous work experience in pharmaceutical or cGMP manufacturing beneficial. VALIDATION ENGINEER Develop protocols and procedures. Execute protocols, review and analyze data for reports. Develop and support validation master plan. Provide support to increase efficiency of operation. Perform validations of utilities and equipment, including redlining of drawings. BSChE or BSME and 3-5 years validation experience preferred; cGMP knowledge required.
Pharmaceutical Associates workweek is Mon-Thur (40 hrs) Benefit package includes medical, dental, vision, and life insurance, 401(k)plan, 6 holidays (10 hr. days), vacation plan. Please send resumes to: Pharmaceutical Associates, Inc., 201 Delaware St. Greenville, SC 29605 Attn: Human Resources

Source - Greenville News - Greenville, SC
REQUIREMENTS
Please refer to the Job Description to view the requirements for this job