Engineer Senior

2 weeks ago

Thousand Oaks, United States Belcan Full time
Details:

Job Title: Engineer Senior
Pay Rate: $44.85 /hr.
Location: Thousand Oaks, CA
ZIP Code: 91320
Start Date: Right Away
Keywords: #Engineering #Manufacturing

Benefits:
* Medical / Health Benefits with multiple plan options, Flexible Spending Accounts, Dental and Vision / glasses / prescription contact lens and eye test options available.
* On the job training / cross-training to develop and expand skills, creating opportunity for advancement and personal development. Tuition reimbursement available for relevant development opportunities.
* Life Insurance, disability insurance, and voluntary life insurance for family members available. Accident and critical illness insurance optional.
* Scheduled performance reviews create opportunities for advancement and pay increases.
* We have many success stories from individuals who took advantage of the training, cross-training, and personal development opportunities for advancement. We also have success stories of individuals who desired a reliable, scheduled and consistent career with appropriate work-life balance, health benefits and good job security. Whichever way you define success, this work culture cares about team members and treats each individual with dignity, inclusion, respect and recognition.
* A Referral Program compensates active employees for referring friends and former colleagues when the referral results in hiring the person. Our team has grown with referrals and internal promotions.

Responsibilities:
Senior Engineer - Single Use Technologies

What you will do
Let"s do this Let"s change the world In this vital role, you will be part of the Drug Substance Technology and Engineering group within the Process Development organization. One of the primary responsibilities will be providing technical leadership for Single Use components and assemblies. In this role, you will also introduce new technologies to the network and will be supporting investigations of Client's global manufacturing.

Other Key Responsibilities Include:
Support of Single Use network in terms of design and investigation
Use process engineering and equipment design experience, to assess unit operation performance and work with both suppliers and the internal network to resolve equipment and single use consumable challenges.
Analyze available data, research technical subjects, and work with other subject matter experts to support resolution of critical investigations.
Provide leadership on capital projects.
Provide process development representation on capital projects, ensuring process requirements are incorporated into equipment and facility designs.
Support and/or lead design of flexible manufacturing equipment and single use consumables, including support of factory acceptance testing and onsite commissioning and qualification.
Support the Client single use global network as a drug substance domain expert.
Provide leadership on various work streams related to improving robustness of design, specification, and qualification of single use consumables and equipment.
Lead technical assessments for supplier and internally inspired changes, evaluating impact to fit and function.
May support technical visits to evaluate capabilities of current and potential suppliers, and assess new technologies that could provide cost, throughput, or other unique capabilities to Client manufacturing.

This role will be mostly remote, with the occasional need to be on site. The person in this position is required to be located within 100 miles of Cambridge, MA or Thousand Oaks, CA.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The detail oriented professional we seek is a highly skilled problem solver with these qualifications.

Basic Qualifications:
High school diploma/GED and 12 years of Engineering or Operations experience OR
Associate"s degree and 10 years of Engineering or Operations experience OR
Bachelor"s degree and 5 years of Engineering or Operations experience OR
Master"s degree and 3 years of Engineering or Operations experience OR
Doctorate degree

Preferred Qualifications:
Master"s degree and 6+ years of directly related experience, or PhD with 2+ years of directly related experience
Strong understanding of GMP equipment design and biologics manufacturing requirements
Detailed knowledge of multiple unit operations
Experience leading root cause analyses and solving GMP manufacturing issues
Ability to apply sophisticated problem solving skills within defined constraints
Experience providing process engineering support of pilot/clinical/commercial processes
Experience with large capital projects, including design, procurement, commissioning and qualification of production scale equipment
Experience with single-use component design and application in biopharmaceutical production
Experience developing and transferring process technology into GMP production environment
Excellent technical writing and verbal communication skills
Excellent facilitation and influencing skills

Thrive
Some of the vast rewards of working here

As we work to develop treatments that take care of others, we also work to care for our teammates" professional and personal growth and well-being.

Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan-comprising health, finance and wealth, work/life balance, and career benefits-with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

EOE/F/M/D/V

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