Utilize client systems to document, track, and fulfill solution preparation orders.
Comply with all GxP regulations, safety requirements, and documentation procedures while performing assigned tasks.
Collect, maintain, and report operational and performance metrics as required by management.
Identify and escalate unsafe conditions or compliance concerns and support timely corrective actions.
Cross-train team members and perform additional duties as needed to support business continuity.
Required Qualifications
Associate’s degree or equivalent relevant experience.
5+ years of laboratory support experience within the biopharmaceutical industry.
Experience with buffer and media preparation processes in laboratory or manufacturing environments.
Proven ability to operate laboratory equipment and follow approved maintenance and safety procedures.
Strong communication skills with a high level of attention to detail.
Demonstrated ability to build relationships and provide excellent customer service to scientific stakeholders.
Proficiency with client systems, including Electronic Laboratory Notebooks (ELNs), and Microsoft Office applications.
Preferred Qualifications
Experience supporting Manufacturing Science & Technology or Process Development teams.
Familiarity with biologics development workflows and laboratory operations.
Ability to contribute effectively to operational reporting and performance metrics.
Strong problem-solving and troubleshooting capabilities in a laboratory setting.
Demonstrated flexibility and ability to adapt to changing business needs and priorities.
Experience working in highly regulated GxP environments.
Proven ability to collaborate effectively across cross-functional teams.
Location: Onsite
Work Shift: 08 Hour Day - 1st Shift/Morning Shift
#LI
This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without sponsorship.
Expected compensation for this position
52,000.00 – 56,160.00 USD per year
Final compensation packages are determined by various considerations including but not limited to candidate qualifications, location, market conditions, and internal considerations.
Location
On-site –Devens, MA
If this job description resonates with you, we encourage you to apply, even if you don’t meet all the requirements. We’re interested in getting to know you and what you bring to the table!
Personalized benefits that support personal well-being and growth
JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits include:
401(k) plan with matching company contributions
Comprehensive Medical, Dental & Vision Care
Paid parental leave at 100% of salary
Paid Time Off and Company Holidays
Early access to earned wages through Daily Pay
At JLL, we harness the power of artificial intelligence (AI) to efficiently accelerate meaningful connections between candidates and opportunities. Using AI capabilities, we analyze your application for relevant skills, experiences, and qualifications to generate valuable insights about how your unique profile aligns with the specific requirements of the role you're pursuing.
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For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here.
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Pursuant to Columbia, SC ordinance, this position is subject to a background check for any convictions directly related to its duties and responsibilities. Only job-related convictions will be considered and will not automatically disqualify the candidate.
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Accepting applications on an ongoing basis until candidate identified.
