Dawar Consulting
Job Description
Our client, a world leader in diagnostics and life sciences, is looking for a
"Sr Manufacturing Engineer
"
based out of
Branchburg, NJ.
The Senior Manufacturing Engineer will lead and manage projects within filling and packaging manufacturing streams. This role focuses on defining equipment specifications, improving process efficiency, reducing downtime, and supporting automation initiatives to ensure compliance, quality, and operational excellence in a cGMP environment.
Responsibilities Plan, design, and implement new manufacturing equipment and packaging processes. Lead cross-functional project teams to meet cost, quality, and performance goals. Support equipment qualification (IQ/OQ/PQ), testing, and validation activities. Develop and maintain manufacturing documentation, including SOPs and process records. Identify opportunities for process optimization, automation, and cost reduction. Ensure compliance with cGMP, ISO, and FDA regulations. Required Skills Bachelor's degree in Engineering or related field. 5-6 years of experience in a
cGMP manufacturing environment
with automated filling and packaging systems. Strong knowledge of
equipment qualification (IQ/OQ/PQ)
and process validation. Proven ability to manage multiple projects in a matrixed organization. Excellent analytical, troubleshooting, and communication skills. Preferred Skills Master's degree in Engineering or related discipline. Experience with
automation, surface treatments, adhesive bonding, microdispensing , and
injection molding . Familiarity with
medical device or diagnostics manufacturing
and
design transfer activities . Knowledge of
Material Science
and continuous improvement methodologies.
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K
Interested Candidates please share your resume to hr@dawarconsulting.com/Kavitha@dawarconsulting.com
Skill Set Process Engineering, Validation
"Sr Manufacturing Engineer
"
based out of
Branchburg, NJ.
The Senior Manufacturing Engineer will lead and manage projects within filling and packaging manufacturing streams. This role focuses on defining equipment specifications, improving process efficiency, reducing downtime, and supporting automation initiatives to ensure compliance, quality, and operational excellence in a cGMP environment.
Responsibilities Plan, design, and implement new manufacturing equipment and packaging processes. Lead cross-functional project teams to meet cost, quality, and performance goals. Support equipment qualification (IQ/OQ/PQ), testing, and validation activities. Develop and maintain manufacturing documentation, including SOPs and process records. Identify opportunities for process optimization, automation, and cost reduction. Ensure compliance with cGMP, ISO, and FDA regulations. Required Skills Bachelor's degree in Engineering or related field. 5-6 years of experience in a
cGMP manufacturing environment
with automated filling and packaging systems. Strong knowledge of
equipment qualification (IQ/OQ/PQ)
and process validation. Proven ability to manage multiple projects in a matrixed organization. Excellent analytical, troubleshooting, and communication skills. Preferred Skills Master's degree in Engineering or related discipline. Experience with
automation, surface treatments, adhesive bonding, microdispensing , and
injection molding . Familiarity with
medical device or diagnostics manufacturing
and
design transfer activities . Knowledge of
Material Science
and continuous improvement methodologies.
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K
Interested Candidates please share your resume to hr@dawarconsulting.com/Kavitha@dawarconsulting.com
Skill Set Process Engineering, Validation