What are the responsibilities and job description for the Regulatory labelling specialist position at Navitas Partners, LLC?
Title: Regulatory labelling specialist
Duration: 12 months
Location: Millsboro, DE
Job Description:
Responsibilities:
- Client Animal Health is a Biotechnology Centre of Excellence that manufactures, fills, packages, and distributes vaccines for animals.
- This position is responsible but is not limited to the following duties:
- Prepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance.
- Support regulatory filing submissions with the USDA for both domestic and international product packaging.
- Independently work with internal stakeholders, regulated packaging processes and system workflows to revise or draft new packaging for vaccine biologicals for both US (domestic) and international markets.
- Ensure prompt availability of labels and artworks and liaises with departments such as Marketing, Pharmacovigilance and Technical Services to ensure compliance with established regulations.
- Training with the USDA regulations on packaging, ARTIS computer system and internal processes and workflows for packaging submissions and filing maintenance.
- Training Type: Corporate Development - Coaching
Qualifications:
Minimum Education: Associate degree.
Preferred Education: Bachelor/Master's degree in Life Science.
Required Experience and Skills:
- With Associate, minimum 5-7 years of relevant experience within pharmaceutical labelling experience.
- With Bachelor's, minimum 4-6 years of relevant experience within pharmaceutical labelling experience.
- With Master's minimum 2-5 year of relevant experience within pharmaceutical labelling experience.
- Require someone with scientific background or familiarity with medical terminology.
- Require someone with excellent proofreading skills.
- Proficient in standard computer programs such as Microsoft Office, Excel, Word, Outlook, SharePoint, ADOBE.
- Preferred/nice to have: Industry - Pharmaceutical Industry/Vaccine manufacturing/Medical and Biotechnology
Personality:
- Attention to details.
- Team Player.
- Able to follow directions.
- Can work independently once the trainings are complete.
- Able to make sure that regulations are met.
- Excellent communication and written skills.
- Open minded.
Must have:
- Regulatory labeling content review as per FDA guideline.
- Quality check of labeling content errors.
- Label artwork, label design review.
- Support the preparation of labeling documents, coordinating labeling document submissions to regulatory bodies.
- Looking for someone with labeling expertise in the pharmaceutical industry, vaccines manufacturing or GMP.
Typical day:
- Very intensive label-oriented job
- Need someone to hit the ground running.
- Label review and submission of labeling documents and artwork
- Label artwork, label design review.
- Quality check for label content and formatting as per FDA guidelines.
- Support the team with the review, revising labeling.
- Attention to details.
- Will prepare the label content following SOP's and FDA regulations.