招聘

Senior Process Engineer- Oral Solid Dose and Finished Goods
Research Triangle Park, NC
·
On-site
·
Full-time
·
1w ago
Compensation
$91,000 - $118,000
Benefits & Perks
•Healthcare
•401(k)
•Equity
•Parental Leave
•Learning Budget
•Gym
•Healthcare
•401k
•Equity
•Parental Leave
•Learning
•Gym
Required Skills
Process Engineering
Oral Solid Dosage
Finished Goods
Equipment Management
Technical Leadership
Regulatory Compliance
About This Role
As a Senior Process Engineer, you will be a key contributor and subject matter expert within the Drug Product Technical Authority supporting Oral Solid Dosage (OSD) & Finished Goods (FG) technologies responsible for driving technical excellence across Biogen’s global manufacturing network. This pivotal role ensures the optimal performance, availability, and compliance of equipment and systems supporting device assembly, labelling, packaging, and oral solid dosage drug product operations. These areas cover both large molecule injectables and devices as well as small molecule, which includes blistering and bottling operations. You will collaborate closely with site engineering leads, providing guidance and oversight to engineering teams, and driving modality development, enhancement, and governance. Your expertise will optimize operations and deliver value to the business, maintaining a strong position within Biogen’s global framework.
This is a hybrid role to be based at our offices in Research Triangle Park, NC.
What You’ll Do
-
Establish and update engineering standards and best practices for all manufacturing sites, covering both Oral Solid Dosage (OSD) and Finished Goods (FG) operations.
-
Lead technical assessments, Facility Fit Feasibility Studies and process improvement initiatives for informed decision-making by senior leadership
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Integrate engineering considerations into new projects and participate in capital planning for both Finished Goods and Oral Solid Dosage.
-
Support the execution of Capital projects inline with the OSD and FG modality requirements and Capital Project Management processes. Support tech transfers for OSD as necessary from an engineering & facilities standpoint.
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Provide direction and support to site engineering teams, ensuring program adherence and technical excellence in both domains.
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Implement continuous improvement strategies for equipment and system performance.
-
Investigate innovative technical, equipment and process solutions, benchmark against industry best practice and alignment.
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Support development of business cases requiring capital investment and participate in capital planning for related project opportunities.
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Engage with external vendors and industry experts for insights into new and innovative technologies relevant to both Finished Goods and Oral Solid Dosage manufacturing.
-
Employ a data-centric approach to engineering for both Finished Goods and Oral Solid Dosage assets.
-
Ensure regulatory compliance, adherence to standards, and alignment with company policies for all engineering activities.
Who You Are
You are an experienced engineer with a solid background in process engineering, experienced in both Oral Solid Dosage and Finished Goods manufacturing. You are a strategic thinker, equipped to serve as a technical SME, and thrive on data-driven analysis to deliver innovative technical solutions.
Qualifications
Required Skills:
-
BS in engineering (mechanical, chemical, electrical, industrial) or related discipline.
-
Minimum 4 years’ experience in Engineering/Maintenance in Biotech, Pharma, Medical Device, or similar manufacturing industry.
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Experience in either Oral Solid Dosage or Finished Goods (device assembly, labelling, packaging). Highly preferred to have experience in both.
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Effective at influencing both site and enterprise levels.
-
Strong communication, presentation, and technical skills.
-
Expertise in core engineering principles.
Preferred Skills:
-
Master’s in Engineering.
-
Engineering & Architectural firm (A+E) experience in the study and design of processes for FG and/or OSD modalities.
Job Level: Professional
Additional Information:
The base compensation range for this role is: $91,000.00-$118,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Short- and Long-Term Disability insurance
- A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 80 hours of sick time per calendar year
- Paid Maternity and Parental Leave benefit
- 401(k) program participation with company matched contributions
- Employee stock purchase plan
- Tuition reimbursement of up to $10,000 per calendar year
- Employee Resource Groups participation
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
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About Biogen

Biogen
PublicSpecializing in the treatment of neurological diseases.
5,001-10,000
Employees
Cambridge
Headquarters
Reviews
4.1
47 reviews
Work Life Balance
3.6
Compensation
4.7
Culture
4.1
Career
4.4
Management
3.8
84%
Recommend to a Friend
Pros
Opportunities for continuous learning and growth
Strong engineering culture with focus on code quality
Cutting-edge technology stack and interesting technical challenges
Cons
Organizational changes and restructuring can be disruptive
Fast-paced environment with tight deadlines
Work-life balance can be challenging during product launches
Salary Ranges
541 data points
Mid/L4
Senior/L5
Mid/L4 · SR Analyst, R&D Business Ops
1 reports
$131,388
total / year
Base
$114,250
Stock
-
Bonus
-
$131,388
$131,388
Interview Experience
47 interviews
Difficulty
3.5
/ 5
Duration
14-28 weeks
Offer Rate
36%
Experience
Positive 65%
Neutral 25%
Negative 10%
Interview Process
1
Phone Screen
2
Technical Interview
3
System Design
4
Behavioral
5
Team Fit
Common Questions
Tell me about a challenging project
System design question
Coding problem
Why this company
News & Buzz
FDA grants breakthrough therapy designation to Biogen’s litifilimab - Investing.com
Source: Investing.com
News
·
5w ago
Biogen’s Litifilimab Receives FDA Breakthrough Therapy Designation for Cutaneous Lupus Erythematosus, a Disease With No Targeted Treatment Options - Biogen
Source: Biogen
News
·
5w ago
FDA Accepts LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease under Priority Review - Biogen
Source: Biogen
News
·
5w ago
Biogen’s Alisha Alaimo On The Company’s Next Big Commercial Build - Citeline News & Insights
Source: Citeline News & Insights
News
·
6w ago