Job Description
The candidate will work in a highly collaborative team environment and be responsible for both moderately complex to complex nGMP and GMP manufacturing activities to support our early phase clinical pipeline of synthetic drug products.
Responsibilities:
- Perform cleaning, sanitization, and setup of processing equipment and process rooms
- Support in Manufacturing Process readiness activities
- Supporting the day to day operational needs of the facility
- Identify, recommend, and implement improvements related to routine functions
- PPE familiarity and ability to use a PAPR
- Ability to work with Microsoft Word, Excel, and PowerPoint
Skills:
- Strong technical skills to support problem solving exercises.
- Strong interpersonal skills and a proactive leadership mindset
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- Excellent verbal and written communication skills
- Ability to adhere to current Good Manufacturing Practices cGMPs and follow Standard Operating Procedures SOPs.
- Understanding of typical unit operations for the manufacture of synthetics drug product (i.e. granulation, roller compaction, drying, milling, blending, compression, encapsulation and film coating)
Education:
- Associate degree in science/pharmaceutical science-related area
Compensation:
The pay rate range above is the base hourly pay range that Aditi Consulting reasonably expects to pay someone for this position (compensation may vary outside of this range depending on a number of factors, including but not limited to, a candidate’s qualifications, skills, competencies, experience, location and end client requirements).
Benefits and Ancillaries:
Medical, dental, vision, PTO benefits and ancillaries may be available for eligible Aditi Consulting employees and vary based on the plan options selected by the employee.