Technical Services Specialist Livermore

Alcon3Pl; Livermore (CA); On-site; USD 41,000 - 52,000; Full time

Benefits offered by this job

Competitive Pay

Health & Wellness

401(k) with company match

Time Off

Job summary

Alcon3Pl is seeking a Technical Services Specialist (Quality Assurance) in Livermore, CA to own raw material and supplier qualification lifecycle for dietary products. Work with R&D and Quality to ensure safety, quality, and regulatory compliance.

Responsibilities include managing supplier documentation, supporting certifications, creating Master Manufacturing Records, and coordinating cross-functional collaboration for product development and launches.

Qualifications

• Bachelor’s degree in Food Science, Chemistry, Biology, or a related field.
• 1–2 years of experience in the nutritional or dietary supplement industry preferred.
• Strong attention to detail and organizational skills; familiarity with GMP, FDA, HACCP, SQF regulations.

Responsibilities

• Lead supplier qualification activities: document collection, review, and approval for new and existing suppliers.
• Support certification programs including Organic, NSF, GFCO, and Non-GMO Project; coordinate regulatory submissions.

Skills

ERP systems

Microsoft Office

Attention to detail

Organizational skills

Education

Bachelor's degree in Food Science, Chemistry, Biology, or related field

Tools

ERP systems

Microsoft Office

Job description

Technical Services Specialist (Quality Assurance)

#128205; Livermore, CA
#127970; Department: Quality Assurance
#128338; Employment Type: Full-Time
#128178; Pay: $30.00 – $38.00 per hour

The Role

We are seeking a detail-oriented Technical Services Specialist to support our Ramp;D and Quality teams in the development and maintenance of high-quality nutritional products.

In this role, you will own the raw material and supplier qualification lifecycle , ensuring all ingredients meet strict safety, quality, and regulatory standards. This is an excellent opportunity for someone looking to grow their career in the dietary supplement or nutritional manufacturing industry.

Key Responsibilities

Supplier Qualification

• Lead document collection, review, and approval for new and existing suppliers
• Ensure supplier compliance with company and regulatory standards

Compliance amp; Certifications

• Support certification programs including Organic, NSF, GFCO, and Non-GMO Project
• Coordinate documentation and submissions for regulatory compliance

Technical Documentation

• Create, review, and maintain Master Manufacturing Records (MMRs)
• Develop and update Finished Product Specifications

Cross-Functional Collaboration

• Partner with Supply Chain, Ramp;D, and Quality teams to support product development and launches
• Ensure smooth communication and execution across departments

Qualifications

• Bachelor’s degree in Food Science, Chemistry, Biology, or a related field
• 1–2 years of experience in the nutritional or dietary supplement industry preferred
• Strong attention to detail and organizational skills
• Proficiency in ERP systems and Microsoft Office (Excel, Word, Outlook)
• Working knowledge of GMP, FDA, HACCP, and SQF regulations

Compensation amp; Benefits

#128178; Competitive Pay: $30.00 – $38.00 per hour
#127973; Health amp; Wellness: Medical, dental, and vision insurance
#128200; Retirement: 401(k) with 4% company match
#127958; Time Off:

• 5 days paid vacation
• 6 days paid sick leave
• 10 paid holidays annually

Growth Opportunities

• Professional development support
• Tuition reimbursement

Why Join Us?

• Work with a collaborative Ramp;D and Quality team
• Be part of a growing company in the nutritional products space
• Gain hands-on experience with regulatory compliance and product development
• Clear path for career growth and advancement