Manufacturing scientist job description

Are you inspired by “what's next”? So are we.

When you join the Albemarle team, you contribute to a better tomorrow. You will play a role in powering many of the world's largest and most critical industries, from energy and communications to transportation and electronics. We are putting innovation to work to improve people's lives and we want YOU to be a part of it.

Job Description

Company and Job Overview

Albemarle Corporation, headquartered in Charlotte, NC, is a leading global producer of lithium, bromine, and catalyst solutions. As one of the world's largest lithium chemicals producers, our products enable today's rapid growth in lithium-ion batteries that power everything from pacemakers, to cell phones, to electric vehicles. Our unique lithium natural resource position, global derivatization capabilities and technology leadership allow Albemarle to execute an aggressive growth strategy. Join us to help develop the technologies and materials that will accelerate the electrification revolution!

The “Lithium Metal Anode Manufacturing Scientist” position is a hands-on role within the fast-growing Lithium R&D team located in Kings Mountain, NC. The successful candidate will join a diverse and passionate team developing new lithium-based products and technologies for Albemarle and its customers.

The Lithium Metal Anode Manufacturing Scientist will spearhead development of advanced lithium metal anodes for current and future generations of high energy density batteries, targeting cost effective manufacturing and cell level performance/useful life. The position requires innovative and hands-on independent laboratory work and collaboration across groups, internally and externally. Success in the position will open career growth opportunities within and outside the R&D team.
Essential Duties & Responsibilities
Design high performance lithium metal anodes by developing anode/foil processing techniques with the ultimate goal of scale-up and commercialization Practice proper laboratory procedures in compliance with Corporate HS&E policies and maintain a safe lab environment Collaborate with a broad technical team and proactively share data to achieve optimal outcomes and meet timebound technical milestones Generate lithium foils and laminates for R&D and customers at the gram to multi-kilogram scale Characterize physical properties of lithium in different forms Document experiments, observations, and results clearly in both written and electronic formats

Required Qualifications
A Ph.D. degree in metallurgy, materials science, chemistry, chemical engineering, mechanical engineering, or related scientific discipline1-3 years of metallurgic experience, including all or some of the following techniques: extrusion, rolling, and lamination of metals At least 1 year of hands-on experience working with lithium metal Strong background in metal processing including melting, alloying, and various processes to shape metal products suitable for customer needs. Experience in rolling and casting is an advantage.Able to find innovative solutions to technical challenges

Desired Competencies
Skilled in safely handling air-sensitive materials Experience with surface metrology and characterization Experience with glovebox operation and working inside a dry room Good understanding of metallography techniques Conversant in the metallurgical literature Knowledge of process automation is an advantage Work cross-functionally in the organization to meet expected deliverables and manage stakeholders Strong organizational and time management skills Excellent communication skills and able to distill complex concepts into clear messages for a wider audience in both formal and informal settings High attention to detail, accuracy, and precision

Physical Requirements
Must be able to work in a chemical laboratory and a dry room environment, which requires standing for 50% or more of the time Must have dexterity to handle small, delicate components and lab equipment Must be able to physically operate lab-scale roll-to-roll equipment Must be able to lift and carry 30-35 pounds

Choose to unlock your full POTENTIAL. Apply today.

**Scientist - External Manufacturing - Chicago, IL or Hackettstown, NJ**

The External Manufacturing Scientist role supports external manufacturing quality initiatives in the region to ensure the ongoing production of high quality and safe food products within the external manufacturing network. This role ensures the implementation of all applicable Mars Global Quality and Food Safety Standards. In addition, supports qualification, product start up, performance management, and process improvement initiatives at Mars Wrigley Confectionary external manufacturing locations. The incumbent will use food science, engineering knowledge, quality management, project management and cost of quality skills to identify opportunities to improve consumer satisfaction, optimize processes and establish measures of quality conformance.

**What are we looking for?**

+ BS degree in Chemistry, Food Science, Engineering or related technical field required

+ Advanced MS degree in Chemistry, Food Science, Engineering or related technical field

+ 2 or more years of quality experience in a food manufacturing facility

+ A minimum of 3 years of experience in a technical area such as Quality & Food Safety, R&D product development, laboratory management quality systems, or food process engineering

+ Excellent interpersonal skills and the ability to work independently and as a member of a team

+ Experienced auditor with accreditation in GFSI Quality systems such as SQF, BRC, FSSC 22000, ISO9000

+ Ability to travel at least 25% of the time

+ ASQ certification

+ Advanced understanding of GMPs, GLPs, HACCP, Sensory, Microbiology, Regulatory and Food law guidelines

**What would your key responsibilities?**

+ Supports the deployment and compliance of the Mars Global EMQM standard and other applicable standards within the External Manufacturing network

+ Supports manufacturing site selection by assessing quality capability and food safety systems performance. Coordinates with the Supply Chain External Manufacturing Team to resolve site selection and audit concerns.

+ Validates new lines and/or capabilities at assigned sites. Initiates, develops, and implements the External Manufacturing Product Risk Assessments (EMPRA) and Technical Specifications (TS 1, 2, 3) for assigned external manufacturers. Ensures robust change management procedure is in place and verified.

+ Provides technical support in statistical analysis, problem solving, product disposition, and risk assessment related to externally manufactured products.

+ Leads audits and follow up on CAPA/CI implementations at the external manufacturing sites

+ Coordinates and leads incident management and investigation for assigned external manufacturers. This responsibility includes initiation of PRIMPs, on-going interpretation and reporting of information from our consumers and customers, executes the business decision regarding product disposition on non-confirming product and incidents which impact food safety.

+ Support Quality Systems operator with managing and executing testing for the product verification program at sites of responsibility

**What can you expect from Mars?**

+ The opportunity to learn and develop, taking charge of your own career across Mars

+ An industry competitive salary and great benefits package

+ Chance to work cross functionally, and add value and impact to the business

+ If you are passionate, a great problem solver, resilient and have a high drive for results, then we want to hear from you!

\#LI-LW1

Carlsbad-CA

At Microbial Manufacturing Services (MMS), a new Business Unit within Thermo Fisher Scientific's Pharma Services Group, we deliver from process development through commercial supply, the expertise, and resources vital to help clients deliver innovative plasmid-based therapeutics as critical raw materials, drug substances, and drug products. Placed in the forefront of our leading and innovative Cell and Gene Therapy businesses enabling clients to cure genetic, rare, and otherwise untreatable diseases as their CDMO of choice.

**How will you make an impact?**

The Scientist III is a shop-floor manufacturing support and execution for biologics manufacturing processes. From new product introduction through process performance qualification, Specialist III is accountable for keeping technical work on track and driving process improvements in collaboration with multi-functional partners. Success in this role means that patients will receive generation lifesaving therapeutics.

**What will you do?**

Provide on-the-floor technical support for critical manufacturing operations.

Expertise and ownership of process/product impacting investigations.

Lead batch record drafting in partnership with other multi-functional SMEs.

Provide hands-on training to manufacturing personnel and ensure multi shift cross-training performed by training matrix for personnel qualification on performing process unit operations.

Support Bill of Materials (BOM) generation in collaboration with client and multi-functional SMEs.

Act as manufacturing technical lead for tech transfers and validation readiness.

Lead process optimization change controls using the TrackWise quality system and coordinate with multi-functional team members to supervise actions and complete project implementations.

Author, review and approve documentation including batch records, protocols, and reports.

Lead all aspects of data management and analysis.

Identify and lead continuous improvement projects.

**How will you get here?**

Technical expertise in a fast-paced and highly technical environment at the groundbreaking of biologics manufacturing. Driving projects to meet daring first-to-market clinical/commercialization timelines while defining standards and driving improvements.

**Education and experience**

B.S. in life sciences, engineering, or a related field + 2 - 4 years experience

M.S. in life sciences, engineering, or a related field + 1 - 2 years experience

Experience in cGMP cleanroom manufacturing and biologics technical operations

Experience in manufacturing operations, engineering, process sciences roles is highly valued.

**Knowledge, Skills, Abilities**

Clear technical communication to diverse internal and team members.

Project management skills including proven track record to deliver technical projects.

Expertise in biologics manufacturing including sophisticated technical topics in upstream and downstream.

Experience in FDA, EMA oversight including deviations investigations, Change Controls, CAPAs, and regulatory inspection audits.

Proven track record to solve sophisticated technical issues and perform advanced data analysis in a multi-functional team.

Standout colleague with proven track record to build consensus and drive performance with diverse partners.

**Benefits:**

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company pension, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

**EEO/Reasonable Accommodation:**

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.