Inteldot
Process Development Sr Associate Scientist (34718)
Inteldot – Puerto Rico
Join Inteldot as a Process Development Senior Associate Scientist.
This role reports to senior leadership and has overall responsibility for a program or project of limited scope.
Responsibilities
Preparation of syringes/vials with cosmetic, particle, or solution defects for developmental studies, equipment characterization, training activities, and commercial equipment set‑up.
Develop and create defects in glass and polymer surfaces; apply innovative, out‑of‑the‑box thinking for cosmetic defect creation on vials and syringes.
Develop, introduce, or improve defect‑creation methods in the laboratory.
Evaluate primary container defective conditions.
Operate laboratory equipment and instruments: micrometer, caliper, microscope, stereomicroscope, analytical balance, pipette techniques, and other lab tools.
Apply aseptic techniques.
Apply 5S and Lean Manufacturing concepts.
Perform visual manual inspection techniques and have experience with manual visual inspection.
Use Microsoft Excel, Smartsheet, and GMP electronic documentation platforms.
Apply problem‑solving/root‑cause analysis tools (5 Whys, Cause and Effect Diagrams).
Provide advanced scientific analysis and troubleshooting skills.
Adhere to cGMP requirements.
Motivate and support the activities of others.
Organize and multitask projects; communicate and collaborate with other departments.
Work in a fast‑paced environment, prioritize multiple tasks, and remain flexible with change.
Strong communication skills; bilingual in English and Spanish.
Qualifications
Master's degree with 3 years of directly related experience or Bachelor's degree with 5 years of directly related experience.
Preferred Bachelor’s degree in engineering.
Structured problem‑solving skills.
Knowledge of cGMP, Lean, 5S, and visual inspection.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Referrals increase your chances of being considered.
#J-18808-Ljbffr
Join Inteldot as a Process Development Senior Associate Scientist.
This role reports to senior leadership and has overall responsibility for a program or project of limited scope.
Responsibilities
Preparation of syringes/vials with cosmetic, particle, or solution defects for developmental studies, equipment characterization, training activities, and commercial equipment set‑up.
Develop and create defects in glass and polymer surfaces; apply innovative, out‑of‑the‑box thinking for cosmetic defect creation on vials and syringes.
Develop, introduce, or improve defect‑creation methods in the laboratory.
Evaluate primary container defective conditions.
Operate laboratory equipment and instruments: micrometer, caliper, microscope, stereomicroscope, analytical balance, pipette techniques, and other lab tools.
Apply aseptic techniques.
Apply 5S and Lean Manufacturing concepts.
Perform visual manual inspection techniques and have experience with manual visual inspection.
Use Microsoft Excel, Smartsheet, and GMP electronic documentation platforms.
Apply problem‑solving/root‑cause analysis tools (5 Whys, Cause and Effect Diagrams).
Provide advanced scientific analysis and troubleshooting skills.
Adhere to cGMP requirements.
Motivate and support the activities of others.
Organize and multitask projects; communicate and collaborate with other departments.
Work in a fast‑paced environment, prioritize multiple tasks, and remain flexible with change.
Strong communication skills; bilingual in English and Spanish.
Qualifications
Master's degree with 3 years of directly related experience or Bachelor's degree with 5 years of directly related experience.
Preferred Bachelor’s degree in engineering.
Structured problem‑solving skills.
Knowledge of cGMP, Lean, 5S, and visual inspection.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Referrals increase your chances of being considered.
#J-18808-Ljbffr