Compunders

Immediate openings for experienced Compounders for Established Sterile Pharmaceuticals Manufacturer at Riverhead, NY manufacturing facility.

Privately held American pharmaceutical manufacturing company located in Riverhead, NY. Proven Management Team with decades of experience and knowledge. Managers and key employees provide hands-on training to employees. Great opportunity for career development and professional growth.

Qualifications:

Candidates must have a High School diploma or equivalent. Candidates with college degrees preferred.

Minimum of 5 years of experience as compounder in the pharmaceutical industry. High level of proficiency with executing and conforming with established manufacturing instructions and established equipment cleaning/sanitization procedures.

High level of proficiency with weighing and transfer of materials.

High level of proficiency with cGMP compliance.

Strong math skills and documentation skills.

Candidates with sterile manufacturing operations experience preferred.

Salary and Benefits:

Salary Range: starts at $30/hour (salary commensurate with experience)

Standard Benefits Include: enrollment in medical insurance after 3 months continuous full time employment; 1 week paid vacation accrues after 1 year of continuous full time employment; 2 weeks paid vacation accrues after 2 years of continuous full time employment; 6 paid holidays (New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving Day and Christmas Day) available after 6 months continuous full time employment; 40 hours per year paid sick time, accessible in blocks of 4 and 8 hours.

Responsibilities include:

Weigh and transfer raw drug substances and excipients in conformance with cGMPs.

Execute bulk manufacturing instructions in conformance with cGMPs.

Execute cleaning and sanitization of bulk manufacturing equipment (i.e. tanks, transfer hoses, pumps, ball joints) procedures in conformance with cGMPs. Execute post-cleaning sampling (i.e. rinsate, swab) procedures in conformance with cGMPs.

Document production activities in conformance with cGMPs.

Execute set-up and breakdown of manufacturing equipment (i.e. tanks, transfer hoses, pumps, ball joints) procedures in conformance with cGMPs.

Successfully complete process for qualification for entry and activity in sterile manufacturing area.

Company Profile: Established (over 25 years in operation) Sterile drug product manufacturer with ISO 5/6/7/8 Clean rooms, Micro and Chemistry labs, and packaging and serialization facilities. Facility specializes in sterile ophthalmic products. Product profile includes approved and monograph products, both prescription and OTC. Operations include company owned trade label, private label and contract manufacturing.

Please submit resumes to: [email protected]