4 часа назад
Supervisor, Tech Transfer (Pharmaceutical Manufacturing)
73 614 - 103 528$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Supervisor, Tech Transfer (Pharmaceutical Manufacturing): Leading technology transfer, product modernization, validation, and manufacturing support activities at a pharmaceutical site with an accent on process scale-up, equipment and process validation, and regulatory documentation. Focus on coordinating cross-functional projects, translating development findings into manufacturing and cleaning processes, and assessing manufacturing changes through risk assessments.
Location: Wilson, North Carolina, United States; onsite
Salary: $73,614–$103,528 per year, plus eligibility for a bonus plan with a 6% target
Company
provides pharmaceutical and healthcare products and services.
What you will do
- Supervise 3–4 direct reports, maintain development plans, provide day-to-day direction, and support employee training.
- Lead technology transfer activities involving process scale-up, new equipment and procedures, equipment and process validation, and development, stability, cleaning, and product validation batches.
- Project manage new product, product modernization, and product transfer projects, coordinating requirements with internal departments, external customers, and vendors.
- Translate development findings into manufacturing and cleaning processes and implement robust manufacturing and technology transfer practices.
- Review, author, and approve technology transfer documents, protocols, tables, final reports, and regulatory submission materials.
- Assess manufacturing changes, prepare risk assessments, and provide technical support for investigations, action plans, and material change requests.
Requirements
- Must work onsite in Wilson, North Carolina, United States.
- Experience coordinating technology transfer, manufacturing, process scale-up, and validation activities.
- Ability to manage projects related to new products, product modernization, and product transfers.
- Ability to review and author technical documentation, execute protocols, and support regulatory submissions and CMC submissions.
- Strong verbal and written communication skills for collaboration with plant, corporate, regulatory, support, and project teams.
- Ability to provide technical direction, support investigations, assess manufacturing changes, and conduct risk assessments.
Culture & Benefits
- Medical, prescription drug, dental, and vision coverage.
- 401(k) plan with company contributions.
- Paid vacation, holidays, and personal days.
- Life insurance, disability coverage, wellness program, and employee assistance program.
- Participation in leadership training.
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