Jobs at Adcock Ingram

Qualifications/experience:

• Pharmacy Bachelor’s degree or equivalent in life sciences or technology-related discipline with minimum 2 years Regulatory Operations experience required.

OR

• Grade 12 with at least 5 years pharmaceutical industry experience, with prior Regulatory Operations experience required.
• Experience leading the management of projects/timelines and collaborating with team members
• Expertise in the use of a document management, eCTD format and regulatory submission requirements and eCTD publishing systems
• Advanced technical skills in best business practices for electronic regulatory document preparation and submission, and document and life cycle management systems
• Previous experience developing work instructions and generating SOP’s that are consistent with health authority requirements and company business practices
• Proven ability to manage, streamline and collaborate to improve document preparation and management systems

Key Job Outputs 

• Responsible for overseeing and guiding the operations of teams managing the creation, assembly, and publishing of electronic submissions, including New  Product Applications and Life Cycle Amendments.
• Represents Regulatory Operations on project teams for matters relating to electronic submissions, driving timelines and deliverables related to submission documents.
• Maintain working knowledge of the regulations and processes that govern the content and maintenance of controlled documents required by the Health  Authorities, ICH and internal working practices.
• Liaise with functional source areas (clinical, quality, regulatory) to ensure documents are compliant with authoring style guide. Work with regulatory document authors to achieve resolution and ensure that documents comply with regulatory and company guidance/template specifications.
• Supports and/or leads the development, refinement, and implementation of internal processes, procedures, work instructions and training programs for  submission production and operational support activities to the RA Systems Department. As needed, trains colleagues and project teams.
• Ensure alignment of personal and company values.

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Key Job Outputs

• Perform pouching of units on the line.
• Conduct filling of products.
• Able to understand process of printing of bags.
• Assist in loading and sealing of units.
• Follow SOP process for Products.
• Follow correct GMP and gowning process
• Inspect units for missing parts/illegible print and fill volumes
• Remove defective units and over pouches.
• Assist in material handling activities.
• Assist in other departmental needs on a daily basis.
• Perform cleaning activities in the department as required per SOP.

Requirements

• Grade 12 or equivalent
• 1 to 2 years’ working experience.
• Experience in pharmaceutical industry – advantageous