With a location in Fort Washington, McNeil Consumer Healthcare, a division of Johnson & Johnson, provides sales, marketing, and logistical services to U.S. retail customers on behalf of the U.S. consumer companies.

The company represents one point of contact with customers for selling teams, customer service, distribution, retail merchandising, and professional detailing. J & J develops and markets baby care, oral care, wound care, and skin care products that address the needs of consumer and healthcare professionals and incorporates the latest innovations.

Clinical Supplies Manager

This position is responsible for all activities related to global OTC Clinical Supplies including planning, execution of packaging, labeling, distribution, return, and destruction of investigational supplies for human use and/or cGxP studies. He/she must be compliant with cGxP and regulatory requirements. The person must serve as subject matter expert with internal customers to support business objectives.

The ideal candidate has a bachelor’s degree, though a master’s degree is preferred. He/she must have eight years of professional work experience, as well as experience with supplies, vendors (CMOs), clinical operations, new product development, quality assurance, medical, regulatory affairs, and project management.

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Quality Assurance Associate (Investigations)

This position provides support to the investigation process that pertains to the manufacturing and packaging operations in addition to guidance on compliance and good manufacturing practice to meet J&J standards and regulatory expectations. He/she will use the investigation process to identify significant compliance and housekeeping issues and prioritize for action. The person will assure that all compliance issues pertaining to manufacturing and packaging operations are properly investigated and that corrective actions are devised to prevent recurrence.

The ideal candidate has a minimum of a bachelor’s degree, preferably focused in biology, chemistry, or other related sciences. He/she must have at least four years experience in the pharmaceutical, OTC, medical device, and/or a biological industry. Experience with LIMS, SAP-QM, EtQ, and statistical analyses tools is preferred.

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Specialist, R&D Quality & Compliance

This position is responsible for documentation quality review/approval or audits, documentation maintenance and archival, quality inspections of product, and participating on internal assessments. He/she participates on R&D project teams as the Quality representative and works with the groups relative to GMP issues, project plans, due dates, and problem identification and resolution along with assisting in compiling documentation to release R&D studies. The person also provides GMP documentation review and approval of batch records and related documents.

The ideal candidate has at minimum a bachelor’s degree in chemistry, biology, engineering, or related science or technical discipline. He/she also has at least three years experience in a regulated laboratory environment. Laboratory documentation review and revision experience is preferred.

Click here to read more about the Specialist, R&D Quality & Compliance position at J&J.