Constance Strothers

Newark, New Jersey, *****

973-***-****

acw027@r.postjobfree.com

A recent degree in Business Management with over 15 years of experience in the Pharmaceutical Industry, Ensure that all phases of manufacturing activity are performed in a safe manner, and in compliance with cGMP and Standard Operating Procedures (SOP's). Effective communication skills both verbal and written.

Team Building & Leadership Staff Development Communication

Quality Assurance Audit Compliance Safety Standards Research & Troubleshooting

PowerPoint Presentations Problem Solving Policy Enforcement

PROFESSIONAL EXPERIENCE

ACTAVIS PHARMACEUTICAL, Edison, New Jersey 2004-Present

Global specialty pharmaceutical company, with over 17,000 employees, operating in 100 countries.

(Experience) Pharmaceutical Operator:

Monitors, organizes and supervise all functions associated with filling and packaging of all products and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations. Work seamlessly with Line Leaders and Technicians in ensuring compliant operations within and between shifts.

Ensure compliance with CGMP regulations and company procedures for drug product packaging and labeling operations. Review and approve batch documentation associated with packaging labeling of medicinal products such as executed batch records, label proof and label text, and other documentation as needed.

Enforce plant safety regulations and Housekeeping practice and encourage employees to become safety conscious.

Supervised, trained and motivated a diverse team of hourly personnel

Build effective relationships with all internal departments to produce superior products.

Performs responsibilities associated with department hiring, training, problem resolution, work assignment delegation, and attendance tracking.

Assures that manufacturing operations are performed in compliance with batch records, SOP's, and cGMP's.

SCHERING-PLOUGH, Kenilworth, New Jersey 2000-2004

US-based pharmaceutical company founded in 1851, now known as Merck & Co.

(Lead) Pharmaceutical Operator

Conduct routine and non-routine analyses of in-process materials, raw materials, Improves the efficiency of the operation by analyzing and correcting production equipment and processing problems; troubleshoots equipment by making minor adjustments.

Show a bias for action and demonstrate a can- do attitude by being a self-starter with demonstrated passion.

Investigate or report questionable test results.

Ensure timely review and completion of accurate data entry in batch records and logbooks

Perform visual inspections of finished products.

Investigate and prepare out of specification reports and customer complaints related to production in Track wise program.

FORMAL EDUCATION

Bachelor of Science in Business Management (2015)

Berkeley College – Newark, New Jersey

TECHNICAL SKILLS

Microsoft Office (Word, Excel, PowerPoint, Outlook, Project)