Job description

Senior Scientist

Pharmaceuticals

Start date: ASAP

$100-115k DOE + 10% annual bonus

New Brunswick, NJ

Relocation assistance offered

We are working with a leading Pharmaceuticals company who have an exciting opportunity for a Senior Scientist to join their growing team in the New Jersey facility. This position will be responsible for ensuring the correct technical scientific principals are followed and industry standards are met. You will also be technical support for the validation program and quality department. An exciting opportunity to be a leader and have people report to you.

Key Responsibilities:

• Design and supervise execution of DOE’s, process optimization studies, and process qualification batches, Process data compilation and analysis using statistical tools.
• Ensure a strong documentation package developed, involving from conceptual study to various phases of product development like process study, characterization, and process qualification and cleaning validation.
• Review of Master batch records, Exhibit Batch protocols, pre-validation and process validation documentation and reports.
• Support documentation preparation for regulatory purposes and stay current on regulatory requirements that have impact on manufacturing processes and evaluate/implement changes if required.
• Provide support and troubleshooting to manufacturing operations as well as identify process improvements and capacity constraints and design and execute projects to support corporate goals. Identify and define project and process improvement opportunities.
• Champion compliance investigations, commitments (CAPA), and change controls.
• Participate on cross-functional team that address specific problems, facilitate discussion and research, enabling procedures to become more efficient, and to build and enhance interdepartmental relationships.
• This is supervisory position with direct reports so part of the responsibilities will be team growth and setting objectives and being a mentor.

Preferred Qualifications:

• Minimum 8 years of experience in Solid oral Manufacturing or Process development.
• Experience in Solid oral dosage development a plus.
• Minimum Masters in Pharmacy, Pharmaceutical Sciences, Chemical Engineering or similar.
• Knowledge of Statistical process control a plus.
• You need to be a confident & interactive team member with able to collaborate with colleagues and stakeholders.
• Great project management and problem-solving skills.

Job Type: Full-time

Salary: $100,000.00 - $115,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Relocation assistance
• Retirement plan
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Supplemental pay types:

• Bonus pay

Ability to commute/relocate:

• New Brunswick, NJ 08901: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• Do you require visa sponsorship?

Education:

• High school or equivalent (Preferred)

Experience:

• Solid Oral Manufacturing: 8 years (Preferred)
• Process development: 4 years (Preferred)

Work Location: One location

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